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ANGIOKERATOMA

A literature search at Indiana University, Bloomington, Indiana


The following items were compiled by SilverPlatter and are presented with their generous permission. (See SilverPlatter's Worldwide Library for bibliographic search information.)
MEDLINE EXPRESS (R) 1/97-8/97 1 of 28

TI: Scrotal angiokeratoma in a young man [letter]

AU: Hisa-T; Taniguchi-S; Goto-Y; Teramae-H; Osato-K; Kakudo-K; Takigawa-M

SO: Acta-Derm-Venereol. 1996 May; 76(3): 248-9

ISSN: 0001-5555

PY: 1996

LA: ENGLISH

CP: NORWAY

MESH: Adult-

MESH: *Angiokeratoma-pathology; *Scrotum-; *Skin-Neoplasms-pathology

TG: Case-Report; Human; Male

PT: LETTER

AN: 96393543

UD: 9706

MEDLINE EXPRESS (R) 1/97-8/97 2 of 28

TI: Angiokeratomas: an update.

AU: Schiller-PI; Itin-PH

AD: Department of Dermatology, University Hospital, Basel, Switzerland.

SO: Dermatology. 1996; 193(4): 275-82

ISSN: 1018-8665

PY: 1996

LA: ENGLISH

CP: SWITZERLAND

AB: Angiokeratomas are vascular lesions which are defined histologically as one or more dilated blood vessel(s) lying directly subepidermal and showing an epidermal proliferative reaction. At the center of pathogenesis there is a capillary ectasia in the papillary dermis. The epidermal changes in all forms of angiokeratoma are secondary. The different entities causing vessel ectasia lead to the many clinical variants of angiokeratoma. Current classification distinguishes between widespread forms (angiokeratoma corporis diffusum), which is usually associated with an inborn error of metabolism, and localized forms, which include solitary angiokeratoma, Fordyce's angiokeratoma, angiokeratoma circumscriptum naeviforme and angiokeratoma of Mibelli.

MESH: Angiokeratoma-epidemiology; Angiokeratoma-pathology; Angiokeratoma-physiopathology; Diagnosis,-Differential; Prognosis-; Skin-Neoplasms-epidemiology; Skin-Neoplasms-pathology; Skin-Neoplasms-physiopathology

MESH: *Angiokeratoma-; *Skin-Neoplasms

TG: Human

PT: JOURNAL-ARTICLE; REVIEW; REVIEW,-TUTORIAL

AN: 97147093

UD: 9705

MEDLINE EXPRESS (R) 1/97-8/97 3 of 28

TI: Widespread angiokeratomas and tuberous sclerosis.

AU: Gil-Mateo-MP; Miquel-FJ; Velasco-AM; Pitarch-A; Fortea-JM; Aliaga-A

AD: Department of Dermatoogy, Hospital General Universitario, Valencia, Spain.

SO: Br-J-Dermatol. 1996 Aug; 135(2): 280-2

ISSN: 0007-0963

PY: 1996

LA: ENGLISH

CP: ENGLAND

AB: We report a 29-year-old woman who had prominent cutaneous markers of tuberous sclerosis, with subependymal nodules and renal cysts on computerized tomographic scan, who also showed multiple angiokeratomas widely distributed on the buttocks and posterior thighs. Enzymatic studies ruled out Fabry's disease and other lysosomal storage disorders. This is the first reported association of widespread angiokeratomas and tuberous sclerosis.

MESH: Adult-; Angiokeratoma-pathology; Skin-Neoplasms-pathology; Tuberous-Sclerosis-pathology

MESH: *Angiokeratoma-complications; *Skin-Neoplasms-complications; *Tuberous-Sclerosis-complications

TG: Case-Report; Female; Human

PT: JOURNAL-ARTICLE

AN: 97036026

UD: 9702

MEDLINE EXPRESS (R) 1992-1996 4 of 28

TI: Cutaneous and cerebral haemangiomas associated with eruptive angiokeratomas.

AU: Ostlere-L; Hart-Y; Misch-KJ

AD: Department of Dermatology, Kingston Hospital, Surrey, U.K.

SO: Br-J-Dermatol. 1996 Jul; 135(1): 98-101

ISSN: 0007-0963

PY: 1996

LA: ENGLISH

CP: ENGLAND

AB: We report a patient with multiple cutaneous and cerebral haemangiomas associated with angiokeratomas. As far as we are aware this patient is unique as the association of cutaneous and cerebral haemangiomas with angiokeratomas has not been previously described.

MESH: Brain-Neoplasms-radiography; Hemangioma-radiography; Middle-Age; Tomography,-X-Ray-Computed

MESH: *Angiokeratoma-pathology; *Brain-Neoplasms-pathology; *Hemangioma-pathology; *Neoplasms,-Second-Primary-pathology; *Skin-Neoplasms-pathology

TG: Case-Report; Human; Male

PT: JOURNAL-ARTICLE

AN: 96372553

UD: 9612

MEDLINE EXPRESS (R) 1992-1996 5 of 28

TI: Scrotal angiokeratoma in a young man [letter]

AU: Hisa-T; Taniguchi-S; Goto-Y; Teramae-H; Osato-K; Kakudo-K; Takigawa-M

SO: Acta-Derm-Venereol. 1996 Jan; 76(1): 75

ISSN: 0001-5555

PY: 1996

LA: ENGLISH

CP: NORWAY

MESH: Adult-; Angiokeratoma-complications; Hemorrhage-diagnosis; Hemorrhage-etiology; Skin-Neoplasms-complications

MESH: *Angiokeratoma-diagnosis; *Scrotum-pathology; *Skin-Neoplasms-diagnosis

TG: Case-Report; Human; Male

PT: LETTER

AN: 96282002

UD: 9611

MEDLINE EXPRESS (R) 1992-1996 6 of 28

TI: Laser treatment of recurrent vulvar angiokeratoma associated with Noonan syndrome.

AU: Meyer-WR; Dotters-DJ

AD: Department of Obstetrics and Gynecology, University of North Carolina, Chapel Hill, USA.

SO: Obstet-Gynecol. 1996 May; 87(5 Pt 2): 863-5

ISSN: 0029-7844

PY: 1996

LA: ENGLISH

CP: UNITED-STATES

AB: BACKGROUND: Vulvar angiokeratoma is often confused with other, more common perineal lesions. Chronically elevated venous pressures may contribute to this rare disorder. Laser treatment may lend palliation for several years. CASE: A woman with the characteristic cardiac abnormalities of Noonan syndrome initially responded to Argon laser treatment of vulvar angiokeratoma. Excessive recurrent disease was treated satisfactorily with the Nd:YAG laser. CONCLUSION: Recurrent vulvar angiokeratoma in Noonan syndrome supports the premise that increased persistent central venous pressure may be involved in the disease process.

MESH: Adult-; Angiokeratoma-complications; Palliative-Care; Skin-Neoplasms-complications; Time-Factors; Vulvar-Neoplasms-complications

MESH: *Angiokeratoma-surgery; *Laser-Surgery; *Neoplasm-Recurrence,-Local-surgery; *Noonan-Syndrome-complications; *Skin-Neoplasms-surgery; *Vulvar-Neoplasms-surgery

TG: Case-Report; Female; Human

PT: JOURNAL-ARTICLE

AN: 96200648

UD: 9610

SB: AIM

MEDLINE EXPRESS (R) 1992-1996 7 of 28

TI: Of APACHEs and PALEFACEs [letter; comment]

CM: Comment on: Am J Dermatopathol 1994 Apr;16(2):130-3

AU: Puig-L

SO: Am-J-Dermatopathol. 1995 Apr; 17(2): 209-11

ISSN: 0193-1091

PY: 1995

LA: ENGLISH

CP: UNITED-STATES

MESH: Adolescence-; Diagnosis,-Differential; Endothelium,-Vascular-pathology; Lymphocytes-pathology; Lymphoma,-Small-Lymphocytic-pathology; Plasma-Cells-pathology; Thorax-

MESH: *Angiokeratoma-pathology; *Skin-Neoplasms-pathology

TG: Case-Report; Human; Male

PT: COMMENT; LETTER

AN: 96166795

UD: 9607

MEDLINE EXPRESS (R) 1992-1996 8 of 28

TI: [Angiokeratoma and fucosidosis. Immunohistochemical and ultrastructural study]

TO: Angiokeratomes et fucosidose. Etude immunohistochimique et ultrastructurale.

AU: Venencie-PY; Pauwels-C; Malherbe-V; Perie-G; Landrieu-P

AD: Unite de Dermatologie, Centre Hospitalier General, Saint-Germain en Laye.

SO: Ann-Dermatol-Venereol. 1995; 122(6-7): 432-5

ISSN: 0151-9638

PY: 1995

LA: FRENCH; NON-ENGLISH

CP: FRANCE

AB: INTRODUCTION. Angiokeratoma can lead to diagnoses other than Fabry's disease. We report a case of angiokeratoma in a child with fucosidosis. CASE REPORT. A 7-year-old child with psychomotor retardation presented angiokeratoma located on the penis. Uptake of type I Ulex Europaeus Agglutinin antilectin antiserum was intense in the endothelial structure. This antibody is specific for alpha-L-fucose residues which were thus found in large quantities in the vacuoles of the ultrastructure. The patient also had a major deficiency in leukocyte, serum and fibroblast alpha-fucosidase. COMMENTS. This is a typical case of fucosidosis, a rare hereditary disease with autosomal recessive transmission due to generalized deficiency in alpha-L-fucosidase. Diffuse angiokeratosis should suggest, other than Fabry's disease, fucosidase and other enzyme deficiencies including sialidase, GM1 gangliosidase as well as Kanzaki's disease.

MESH: Angiokeratoma-pathology; Angiokeratoma-ultrastructure; Child-; English-Abstract; Fucosidosis-pathology; Immunohistochemistry-; Skin-pathology; Skin-ultrastructure; Skin-Neoplasms-pathology; Skin-Neoplasms-ultrastructure

MESH: *Angiokeratoma-etiology; *Fucosidosis-complications; *Skin-Neoplasms-etiology

TG: Case-Report; Human; Male

PT: JOURNAL-ARTICLE

AN: 96099543

UD: 9603

SB: NURSING

MEDLINE EXPRESS (R) 1992-1996 9 of 28

TI: Argon laser treatment of cutaneous multiple angiokeratomas.

AU: Occella-C; Bleidl-D; Rampini-P; Schiazza-L; Rampini-E

AD: Department of Dermatology, Istituto Scientifico Giannina Gaslini, Genova, Italy.

SO: Dermatol-Surg. 1995 Feb; 21(2): 170-2

ISSN: 1076-0512

PY: 1995

LA: ENGLISH

CP: UNITED-STATES

AB: BACKGROUND. Angiokeratomas are cutaneous vascular lesions with common clinical and histological features: dark red to black papules and ectasia of upper dermis vessels, respectively. Multiple angiokeratomas are difficult to treat because they are often too extensive for surgery and cautery, procedures frequently leading to hemorrhage and scarring. OBJECTIVE. Our report is designed to evaluate the efficacy of argon laser photocoagulation in the treatment of multiple angiokeratomas. METHODS. Two male patients affected by angiokeratoma circumscriptum and angiokeratoma of Fordyce, respectively, were treated using an argon laser under local anesthesia. The laser beam was used as a hemostyptic and to flatten vascular papules by photocoagulation. RESULTS. The cosmetic results of argon laser treatment were good. Posttreatment crusting lasted 2 weeks; 4 months later there was excellent healing without scarring. CONCLUSION. Angiokeratomas respond favorably to argon laser photocoagulation since vascular ectasias are localized in the papillary dermis. Thus, the argon laser offers significant advantages over traditional methods and produces no side effects.

MESH: Adult-; Angiokeratoma-pathology; Biopsy-; Buttocks-; Chronic-Disease; Remission-Induction; Scrotum-; Skin-pathology; Skin-Neoplasms-pathology

MESH: *Angiokeratoma-surgery; *Laser-Coagulation; *Skin-Neoplasms-surgery

TG: Case-Report; Human; Male

PT: JOURNAL-ARTICLE

AN: 95202320

UD: 9506

MEDLINE EXPRESS (R) 1992-1996 10 of 28

TI: On the discriminatory value of anti-HPCA-1 (CD-34) in the differential diagnosis of benign and malignant cutaneous vascular proliferations.

AU: Suster-S; Wong-TY

AD: Arkadi M. Rywlin Department of Pathology & Laboratory Medicine, Mount Sinai Medical Center, Miami Beach, FL 33140.

SO: Am-J-Dermatopathol. 1994 Aug; 16(4): 355-63

ISSN: 0193-1091

PY: 1994

LA: ENGLISH

CP: UNITED-STATES

AB: The staining pattern of monoclonal antibody anti-HPCA-1 (CD-34) was studied in 95 cases of benign and malignant cutaneous vascular proliferations and compared with other vascular endothelium-associated antigenic markers in paraffin-embedded tissues. The proliferating vessels in 22 cutaneous capillary hemangiomas, 8 lobular capillary hemangiomas, and 1 case of papillary intravascular endothelial hyperplasia stained strongly positively for anti-HPCA-1, and the intensity of the reaction was paralleled by that of factor VIII-related antigen (FVIII), Ulex europaeus lectin-1 (UEA), and vimentin (VIM). The vessels in 10 cases of granulation tissue, 6 cases of cavernous hemangioma, 6 cases of angiokeratoma, 5 cases of angiolymphoid hyperplasia with eosinophilia (epithelioid hemangioma), and 3 cases of bacillary angiomatosis showed a lack of reactivity with anti-HPCA-1 and staining of variable intensity with the other markers. Twenty cases of Kaposi's sarcoma (seven patch, five plaque, eight nodular stage) showed strong labeling with anti-HPCA-1 in small, well-formed vessels scattered among the spindle-cell proliferation, and four of these cases showed focal positivity of scattered spindle cells. Nine cases of cutaneous angiosarcoma, two cases of low-grade epithelioid angiosarcoma, and one case of spindle-cell hemangioendothelioma were negative for anti-HPCA-1 and showed variable reactivity for FVIII and UEA; all cases stained strongly positively for VIM. The results of this study indicate that although anti-HPCA-1 shows a high sensitivity for the staining of normal vascular endothelium, its specificity may be restricted to mature, well-formed vessels, therefore rendering its discriminatory value very limited for the identification of poorly differentiated vascular endothelial neoplasms.

MESH: von-Willebrand-Factor-analysis; Angiokeratoma-blood-supply; Angiokeratoma-diagnosis; Angiomatosis,-Bacillary-diagnosis; Angiomatosis,-Bacillary-pathology; Antibodies,-Monoclonal-diagnostic-use; Diagnosis,-Differential; Endothelium,-Vascular-pathology; Granulation-Tissue-blood-supply; Granuloma,-Pyogenic-diagnosis; Hemangioendothelioma,-Epithelioid-blood-supply; Hemangioendothelioma,-Epithelioid-diagnosis; Hemangioma-blood-supply; Hemangioma-diagnosis; Hemangioma,-Capillary-blood-supply; Hemangioma,-Capillary-diagnosis; Hemangioma,-Cavernous-blood-supply; Hemangioma,-Cavernous-diagnosis; Hemangiosarcoma-blood-supply; Hemangiosarcoma-diagnosis; Hyperplasia-; Lectins-analysis; Paraffin-Embedding; Sarcoma,-Kaposi's-blood-supply; Sarcoma,-Kaposi's-diagnosis; Skin-Diseases,-Vascular-pathology; Staining-; Vimentin-analysis

MESH: *Antigens,-CD-analysis; *Skin-Diseases,-Vascular-diagnosis; *Skin-Neoplasms-blood-supply; *Skin-Neoplasms-diagnosis; *Tumor-Markers,-Biological-analysis

TG: Comparative-Study; Human

PT: JOURNAL-ARTICLE

RN: 0; 0; 0; 0; 0; 0; 0; 0

NM: von-Willebrand-Factor; Antibodies,-Monoclonal; Antigens,-CD; Antigens,-CD34; Lectins; Tumor-Markers,-Biological; Ulex-europaeus-lectins; Vimentin

AN: 95068714

UD: 9502

MEDLINE EXPRESS (R) 1992-1996 11 of 28

TI: Rare palpebral tumours. Histopathological aspects.

AU: Halalau-F; Laky-D

AD: Victor Babes Institute, Bucharest, Romania.

SO: Rom-J-Morphol-Embryol. 1994 Jan-Jun; 40(1-2): 51-3

ISSN: 1220-0522

PY: 1994

LA: ENGLISH

CP: ROMANIA

MESH: Adult-; Angiokeratoma-pathology; Lymphoma,-B-Cell-pathology; Middle-Age; Neoplasm-Recurrence,-Local

MESH: *Eyelid-Neoplasms-pathology

TG: Case-Report; Human

PT: JOURNAL-ARTICLE

AN: 95367666

UD: 9511

MEDLINE EXPRESS (R) 1992-1996 12 of 28

TI: Angiokeratoma corporis diffusum in fucosidosis.

AU: George-S; Graham-Brown-RA

AD: Department of Dermatology, Leicester Royal Infirmary, UK.

SO: J-R-Soc-Med. 1994 Nov; 87(11): 707

ISSN: 0141-0768

PY: 1994

LA: ENGLISH

CP: ENGLAND

MESH: Angiokeratoma-pathology; Child-; Genitalia,-Female-pathology; Skin-Neoplasms-pathology

MESH: *Fabry's-Disease-etiology; *Fucosidosis-complications; *Skin-Neoplasms-etiology

TG: Case-Report; Female; Human

PT: JOURNAL-ARTICLE

AN: 95138992

UD: 9505

MEDLINE EXPRESS (R) 1992-1996 13 of 28

TI: Lack of association between varicocele and angiokeratoma of the scrotum (Fordyce).

AU: Orvieto-R; Alcalay-J; Leibovitz-I; Nehama-H

AD: Department of Obstetrics and Gynecology, Golda Medical Center, Hasharon Hospital, Petah Tiqva, Israel.

SO: Mil-Med. 1994 Jul; 159(7): 523-4

ISSN: 0026-4075

PY: 1994

LA: ENGLISH

CP: UNITED-STATES

AB: Angiokeratoma of the scrotum is thought to be associated with varicocele. Our study population consisted of young soldiers and adult reservists. The young population was screened during routine medical examination for the existence of varicocele or angiomas on the scrotum, while the adult reservists, who according to their medical records had varicocele, were randomly questioned for the existence of any kind of spots or lesions on their scrota. We found no association between varicocele and angiokeratoma of the scrotum. Since the prevalence of varicocele is high, it is possible that in the reported cases the association of varicocele and angiokeratoma of the scrotum was coincidental.

MESH: Adolescence-; Adult-; Middle-Age

MESH: *Angiokeratoma-complications; *Genital-Neoplasms,-Male-complications; *Military-Personnel; *Scrotum-; *Varicocele-complications

TG: Human; Male

PT: JOURNAL-ARTICLE

AN: 95115900

UD: 9504

MEDLINE EXPRESS (R) 1992-1996 14 of 28

TI: Multiple angiokeratomas with zosteriform distribution in two sisters.

AU: Eizaguirre-X; Landa-N; Raton-JA; Diaz-Perez-JL

AD: Department of Dermatology, Hospital de Cruces, Bilbao, Spain.

SO: Int-J-Dermatol. 1994 Sep; 33(9): 641-2

ISSN: 0011-9059

PY: 1994

LA: ENGLISH

CP: UNITED-STATES

MESH: Adult-; Age-of-Onset; Angiokeratoma-genetics; Angiokeratoma-physiopathology; Remission,-Spontaneous; Skin-Neoplasms-genetics; Skin-Neoplasms-physiopathology

MESH: *Angiokeratoma-classification; *Angiokeratoma-pathology; *Skin-Neoplasms-classification; *Skin-Neoplasms-pathology

TG: Case-Report; Female; Human

PT: JOURNAL-ARTICLE

AN: 95095457

UD: 9503

MEDLINE EXPRESS (R) 1992-1996 15 of 28

TI: Acral pseudolymphomatous angiokeratoma. A variant of the cutaneous pseudolymphomas [see comments]

CM: Comment in: Am J Dermatopathol 1995 Apr;17(2):209-11

AU: Kaddu-S; Cerroni-L; Pilatti-A; Soyer-HP; Kerl-H

AD: Department of Dermatology, University of Graz, Austria.

SO: Am-J-Dermatopathol. 1994 Apr; 16(2): 130-3

ISSN: 0193-1091

PY: 1994

LA: ENGLISH

CP: UNITED-STATES

AB: APACHE (acral pseudolymphomatous angiokeratoma of children) is a recently described benign cutaneous condition. Only a few cases have been documented to date. The disease has been previously reported in children between 2 and 13 years of age as unilateral eruptions of multiple angiomatous papules on acral sites of the hands and feet. We herein report two cases of APACHE, one occurring in a 16-year-old boy and the other in a 64-year-old woman. Unlike the previously reported cases, our female patient presented in adulthood with a single lesion on the back. Histopathologic and immunohistochemical investigations reveal characteristic features, allowing APACHE to be included among the group of cutaneous pseudolymphomas.

MESH: Adolescence-; Diagnosis,-Differential; Immunoenzyme-Techniques; Lymphoma,-Small-Lymphocytic-pathology; Middle-Age; Skin-pathology

MESH: *Angiokeratoma-pathology; *Skin-Neoplasms-pathology

TG: Case-Report; Female; Human; Male

PT: JOURNAL-ARTICLE

AN: 94303810

UD: 9410

MEDLINE EXPRESS (R) 1992-1996 16 of 28

TI: Angiokeratoma of Fordyce: a cause of scrotal bleeding.

AU: Taniguchi-S; Inoue-A; Hamada-T

AD: Department of Dermatology, Osaka City University Medical School, Japan.

SO: Br-J-Urol. 1994 May; 73(5): 589-90

ISSN: 0007-1331

PY: 1994

LA: ENGLISH

CP: ENGLAND

MESH: Angiokeratoma-pathology; Genital-Diseases,-Male-etiology; Middle-Age; Scrotum-pathology; Skin-Neoplasms-pathology

MESH: *Angiokeratoma-complications; *Hemorrhage-etiology; *Scrotum-; *Skin-Neoplasms-complications

TG: Case-Report; Human; Male

PT: JOURNAL-ARTICLE

AN: 94282555

UD: 9409

MEDLINE EXPRESS (R) 1992-1996 17 of 28

TI: Angiokeratomas in Fabry's disease and Fordyce's disease: successful treatment with copper vapour laser.

AU: Lapins-J; Emtestam-L; Marcusson-JA

AD: Department of Dermatology, University Hospital, Huddinge, Sweden.

SO: Acta-Derm-Venereol. 1993 Apr; 73(2): 133-5

ISSN: 0001-5555

PY: 1993

LA: ENGLISH

CP: SWEDEN

AB: Two patients with multiple angiokeratomas on genitalia and thighs, one with Fabry's disease and one with Fordyce's disease, were treated with copper vapour laser light of 578 nm wavelength. The result was desirable, with destruction and disappearance of the lesions and minimal scarring and posttreatment hyper- or hypopigmentation.

MESH: Adult-; Aged-; Aged,-80-and-over; Angiokeratoma-etiology; Buttocks-; Copper-; Genitalia,-Male; Skin-Neoplasms-etiology; Thigh-; Treatment-Outcome

MESH: *Angiokeratoma-surgery; *Fabry's-Disease-complications; *Fox-Fordyce-Disease-complications; *Laser-Surgery; *Skin-Neoplasms-surgery

TG: Case-Report; Human; Male

PT: JOURNAL-ARTICLE

RN: 7440-50-8

NM: Copper

AN: 93370068

UD: 9312

MEDLINE EXPRESS (R) 1992-1996 18 of 28

TI: Slides in dermatology: 1.

AU: Leslie-TA; Dowd-PM

AD: University College, London.

SO: Br-J-Hosp-Med. 1993 Oct 6-19; 50(7): 415-6

ISSN: 0007-1064

PY: 1993

LA: ENGLISH

CP: ENGLAND

MESH: Angiokeratoma-diagnosis; Angiokeratoma-pathology; Diagnosis,-Differential; Granuloma-Annulare-diagnosis; Granuloma-Annulare-pathology; Ischemia-diagnosis; Ischemia-pathology; Scleroderma,-Systemic-diagnosis; Scleroderma,-Systemic-pathology; Skin-blood-supply; Skin-pathology; Skin-Diseases-pathology; Skin-Neoplasms-diagnosis; Skin-Neoplasms-pathology

MESH: *Skin-Diseases-diagnosis

TG: Human

PT: JOURNAL-ARTICLE

AN: 94084512

UD: 9403

MEDLINE EXPRESS (R) 1992-1996 19 of 28

TI: [Surface microscopy of pigmented cutaneous tumors]

TO: Microscopie de surface des tumeurs cutanees pigmentees.

AU: Soyer-HP; Kerl-H

AD: Clinique Dermatologique et Venereologique, l'Universite de Graz, Autriche.

SO: Ann-Dermatol-Venereol. 1993; 120(1): 15-20

ISSN: 0151-9638

PY: 1993

LA: FRENCH; NON-ENGLISH

CP: FRANCE

AB: BACKGROUND: Clinical guidelines for the diagnosis of pigmented lesions of the skin are not always reliable. Especially the differential diagnosis between benign dysplastic nevi (Clark's nevi) and early melanomas, as well as between melanocytic and nonmelanocytic skin tumors (seborrheic keratoses, pigmented basal cell carcinomas and angiokeratomas) is often difficult. OBJECTIVE: Surface microscopy, which is performed today under various synonyms (dermoscopy, dermatoscopy, epiluminescence microscopy, incident light microscopy, skin microscopy), has been shown to provide additional features and subtle clues for the assessment of pigmented skin lesions. METHODS: The pigmented lesions are covered in vivo with a drop of immersion oil and a glass slide, and observed in incident light by using a stereomicroscope (magnification 6- to 40-fold) or a hand-held instrument called dermatoscope (magnification 10-fold). The immersion oil renders the stratum corneum translucent and allows a better observation of distinctive alterations of the dermoepidermal junction and the papillary dermis. RESULTS: The various criteria of surface microscopy (e.g. pigment network, black dots or irregular extensions) that cannot be discerned by the naked eye are summarized and discussed in detail. The diagnostic significance but also the limitations of this technique are emphasized. CONCLUSION: Surface microscopy opens up a new dimension of clinical morphology for the diagnosis of pigmented skin tumors and facilitates a more reliable assessment of the lesions.

MESH: Angiokeratoma-pathology; Carcinoma,-Basal-Cell-pathology; Diagnosis,-Differential; English-Abstract; Keratosis,-Seborrheic-pathology; Pigmentation-Disorders-pathology

MESH: *Melanoma-pathology; *Microscopy-methods; *Nevus,-Pigmented-pathology; *Skin-Neoplasms-pathology

TG: Human

PT: JOURNAL-ARTICLE

AN: 93332353

UD: 9310

SB: NURSING

MEDLINE EXPRESS (R) 1992-1996 20 of 28

TI: Angiokeratoma corporis circumscriptum naeviforme with transepidermal elimination.

AU: Miwa-N; Kobayashi-T; Kanzaki-T; Tsuji-T

AD: Department of Dermatology, Nagoya City University Medical School, Japan.

SO: J-Dermatol. 1993 Apr; 20(4): 247-51

ISSN: 0385-2407

PY: 1993

LA: ENGLISH

CP: JAPAN

AB: A 5-year-old Japanese boy visited our clinic for treatment of a dark bluish papulonodular lesion on his right thigh. The histopathology of the lesion indicated angiokeratoma corporis circumscriptum naeviforme. Topical antibiotics were prescribed for occasional bleeding from the site. Frequent bleeding started in April of 1992, when erythema and itching were observed around the angiokeratoma. Histopathology of the lesion showed heavy lymphoid cell infiltration around dilated capillaries and irregular acanthosis engulfing dilated capillaries. Interestingly, there were confined masses of red blood cells in the epidermal layer as well as both in and on the horny layer. This is a feature of transepidermal elimination. This transepidermal elimination appeared to be triggered or enhanced by the concomitant contact dermatitis due to topical antibiotics. To the best of our knowledge, this is the first report of angiokeratoma in which the angiokeratoma itself reduced in size through transepidermal elimination, possibly caused by contact dermatitis.

MESH: Angiokeratoma-blood-supply; Capillaries-pathology; Child,-Preschool; Epidermis-pathology; Erythrocytes-pathology; Neomycin-adverse-effects; Povidone-Iodine-adverse-effects; Skin-Neoplasms-blood-supply

MESH: *Angiokeratoma-pathology; *Dermatitis,-Contact-pathology; *Skin-Neoplasms-pathology

TG: Case-Report; Human; Male

PT: JOURNAL-ARTICLE

RN: 1404-04-2; 25655-41-8

NM: Neomycin; Povidone-Iodine

AN: 93301263

UD: 9309

MEDLINE EXPRESS (R) 1992-1996 21 of 28

TI: Ramon syndrome with diabetes mellitus and vascular skin lesions in two sibs.

AU: Pridmore-C; Baraitser-M; Leonard-J

AD: Department of Clinical Genetics, Institute of Child Health, London, UK.

SO: Clin-Dysmorphol. 1992 Jan; 1(1): 29-35

ISSN: 0962-8827

PY: 1992

LA: ENGLISH

CP: ENGLAND

AB: Two sibs are reported with Ramon syndrome with the previously undescribed associations of insulin dependent diabetes mellitus and vascular skin lesions.

MESH: Adolescence-; Angiokeratoma-genetics; Child-; Diabetes-Mellitus,-Insulin-Dependent-genetics; Facial-Bones-abnormalities; Facial-Bones-radiography; Mental-Retardation-genetics; Skin-Diseases,-Vascular-genetics; Syndrome-; Telangiectasis-genetics

MESH: *Diabetes-Mellitus,-Insulin-Dependent; *Skin-Diseases,-Vascular

TG: Case-Report; Female; Human; Male

PT: JOURNAL-ARTICLE; REVIEW; REVIEW-OF-REPORTED-CASES

AN: 94115528

UD: 9404

MEDLINE EXPRESS (R) 1992-1996 22 of 28

TI: Angiokeratoma of the clitoris: a subtype of angiokeratoma vulvae.

AU: Yamazaki-M; Hiruma-M; Irie-H; Ishibashi-A

AD: Department of Dermatology, National Defense Medical College, Saitama, Japan.

SO: J-Dermatol. 1992 Sep; 19(9): 553-5

ISSN: 0385-2407

PY: 1992

LA: ENGLISH

CP: JAPAN

AB: A 24-year-old married woman had an angiokeratoma of the vulva measuring 3 x 3 x 4 mm localized at the clitoris. The nodule was noticed when she was pregnant with her first child. This tumor grew with occasional tenderness and bleeding during pregnancy, but its size did not change after delivery. The growth of this tumor might be attributable to an increase in venous pressure or serum progesterone levels; therefore this disorder might be classified as a subtype of angiokeratoma of the vulva. This is the first case of angiokeratoma localized at the clitoris.

MESH: Adult-; Angiokeratoma-surgery; Clitoris-surgery; Pregnancy-; Pregnancy-Complications,-Neoplastic-pathology; Vulvar-Neoplasms-surgery

MESH: *Angiokeratoma-pathology; *Clitoris-pathology; *Vulvar-Neoplasms-pathology

TG: Case-Report; Female; Human

PT: JOURNAL-ARTICLE

AN: 93123614

UD: 9304

MEDLINE EXPRESS (R) 1992-1996 23 of 28

TI: Angiokeratoma of the clitoris.

AU: McNeely-TB

AD: Department of Pathology, Vancouver (British Columbia) General Hospital, Canada.

SO: Arch-Pathol-Lab-Med. 1992 Aug; 116(8): 880-1

ISSN: 0003-9985

PY: 1992

LA: ENGLISH

CP: UNITED-STATES

AB: A 25-year-old woman, multigravida, presented with a dark ulcerated tumor of the clitoris. Histologic examination demonstrated an angiokeratoma, a benign telangiectatic vascular tumor. To our knowledge, this is the first report of angiokeratoma of the clitoris and only the fifth describing vascular tumor of this organ. The clinical differential diagnosis of angiokeratoma and of clitoral tumors includes malignant neoplasms such as melanoma. Biopsy with histologic examination is, therefore, recommended to ensure appropriate treatment of these unusual tumors.

MESH: Adult-; Angiokeratoma-diagnosis; Biopsy-; Diagnosis,-Differential; Melanoma-diagnosis; Melanoma-pathology; Vulvar-Neoplasms-diagnosis

MESH: *Angiokeratoma-pathology; *Clitoris-; *Vulvar-Neoplasms-pathology

TG: Case-Report; Female; Human

PT: JOURNAL-ARTICLE

AN: 92359692

UD: 9211

SB: AIM

MEDLINE EXPRESS (R) 1992-1996 24 of 28

TI: Scrotal angiokeratoma (Fordyce): histopathological and ultrastructural findings.

AU: Gioglio-L; Porta-C; Moroni-M; Nastasi-G; Gangarossa-I

AD: Institute of Human Anatomy, University of Pavia, Italy.

SO: Histol-Histopathol. 1992 Jan; 7(1): 47-55

ISSN: 0213-3911

PY: 1992

LA: ENGLISH

CP: SPAIN

AB: Bioptic findings related to four cases of scrotal angiokeratoma-Fordyce, were studied under light and electron microscopy. A particular heterogeneity of the structural and ultrastructural patterns typical of this lesion was thus observed. Light microscopy study pointed out, in particular, different degrees of dilation of papillary vessels, whereas ultrastructural study highlighted marked alterations of endothelial cells with structural and quantitative modifications of cytoplasmic organelles.

MESH: Angiokeratoma-ultrastructure; Endothelium,-Vascular-ultrastructure; Scrotum-ultrastructure; Skin-Neoplasms-ultrastructure

MESH: *Angiokeratoma-pathology; *Endothelium,-Vascular-pathology; *Scrotum-pathology; *Skin-Neoplasms-pathology

TG: Human; Male

PT: JOURNAL-ARTICLE

AN: 92248279

UD: 9208

MEDLINE EXPRESS (R) 1992-1996 25 of 28

TI: Acquired benign and "borderline" vascular lesions.

AU: Hunt-SJ; Santa-Cruz-DJ

AD: Division of Dermatology, University of California, San Diego Medical Center.

SO: Dermatol-Clin. 1992 Jan; 10(1): 97-115

ISSN: 0733-8635

PY: 1992

LA: ENGLISH

CP: UNITED-STATES

AB: In recent years, the classification of vascular lesions has been expanded and modified with the addition of several newly described entities, the redefinition of others, the recognition of lesions of borderline biologic behavior, and the need to avoid misdiagnosis with early Kaposi's sarcoma. This review clarifies the nomenclature, updates information on previously known lesions, and summarizes data on several recently discovered, lesser-known entities such as glomeruloid hemangioma, microvenular hemangioma, and multinucleate cell angiohistiocytoma. Clinicopathologic features and differential diagnosis are emphasized.

MESH: Angiokeratoma-pathology; Angiolymphoid-Hyperplasia-with-Eosinophilia-pathology; Hemangioendothelioma-pathology; Hemangioma-pathology; Telangiectasis-pathology

MESH: *Neoplasms,-Vascular-Tissue-pathology; *Skin-Neoplasms-pathology

TG: Human

PT: JOURNAL-ARTICLE; REVIEW; REVIEW,-ACADEMIC

AN: 92110984

UD: 9204

MEDLINE EXPRESS (R) 1991 26 of 28

TI: Transepidermal elimination of thrombi in three cases of thrombotic angiokeratoma: an incidental histopathologic finding of angiokeratoma.

AU: Bang-DS; Choi-YS; Song-MS

AD: Department of Dermatology, Yonsei University College of Medicine, Seoul, Korea.

SO: J-Dermatol. 1991 Oct; 18(10): 605-9

ISSN: 0385-2407

PY: 1991

LA: ENGLISH

CP: JAPAN

AB: Transepidermal elimination (TEE) is a well known phenomenon by which foreign or altered constituents are removed from the dermis. A thrombosis in the dilated dermal blood vessels of angiokeratoma is not unusual, hence the term thrombotic angiokeratoma. We recently reviewed the histopathologic findings of previously diagnosed cases of angiokeratoma and found that multiple histologic sections of surgical biopsy materials disclosed changes indicating TEE of thrombi in three cases. Special stains searching for an altered substance in those thrombi failed. In this report of three cases, we suggest that this phenomenon could be an incidental and long missed histopathologic finding of angiokeratoma which might explain the fate of these thrombi.

MESH: Adult-; Infant-; Leg-Dermatoses-pathology

MESH: *Angiokeratoma-pathology; *Epidermis-pathology; *Thrombosis-pathology

TG: Case-Report; Female; Human; Male

PT: JOURNAL-ARTICLE

AN: 92166085

UD: 9206

MEDLINE EXPRESS (R) 1991 27 of 28

TI: Two Japanese cases with aspartylglycosaminuria: clinical and morphological features.

AU: Yoshida-K; Ikeda-S; Yanagisawa-N; Yamauchi-T; Tsuji-S; Hirabayashi-Y

AD: Department of Medicine (Neurology), Shinshu University School of Medicine, Matsumoto, Japan.

SO: Clin-Genet. 1991 Oct; 40(4): 318-25

ISSN: 0009-9163

PY: 1991

LA: ENGLISH

CP: DENMARK

AB: Two members of a consanguineous Japanese family with a clinical picture of aspartylglycosaminuria (AGU) are described. Both patients exhibited mental retardation, coarse facial features, angiokeratoma and myoclonic seizures. Biochemical studies showed elevated excretion of urinary sialyloligosaccharides and decreased activity of aspartylglycosaminidase in lymphoblasts. Morphologic studies of skin biopsy specimens showed many clear vacuoles mainly in the vascular endothelial cells and secretory cells of the sweat glands. Osmiophilic lamellar cytoplasmic inclusions were also noted in the ganglion cells in rectal biopsy. The ethnic distribution of AGU may be more widespread than previously suspected and appears not to be restricted to Finnish populations. Ours are the first Japanese patients diagnosed as AGU. We conclude that AGU should also be included in the differential diagnosis of mentally retarded patients in Asian countries.

MESH: Acetylglucosamine-urine; Adult-; Angiokeratoma-genetics; Carbohydrate-Sequence; Epilepsy,-Myoclonic-genetics; Japan-epidemiology; Mental-Retardation-genetics; Molecular-Sequence-Data; Oligosaccharides-urine; Rectum-pathology; Rectum-ultrastructure; Skin-Neoplasms-genetics

MESH: *Acetylglucosamine-analogs-and-derivatives; *Aspartylglucosylaminase-deficiency

TG: Case-Report; Female; Human

PT: JOURNAL-ARTICLE

RN: EC 3.5.1.26; 0; 0; 2776-93-4; 7512-17-6

NM: Aspartylglucosylaminase; sialooligosaccharides; Oligosaccharides; N-acetylglucosaminylasparagine; Acetylglucosamine

AN: 92097321

UD: 9204

MEDLINE EXPRESS (R) 1991 28 of 28

TI: Acral pseudolymphomatous angiokeratoma of children (APACHE): a case report and immunohistological study.

AU: Hara-M; Matsunaga-J; Tagami-H

AD: Department of Dermatology, Tohoku University School of Medicine, Sendai, Japan.

SO: Br-J-Dermatol. 1991 Apr; 124(4): 387-8

ISSN: 0007-0963

PY: 1991

LA: ENGLISH

CP: ENGLAND

AB: Acral pseudolymphomatous angiokeratoma of children (APACHE) is a new clinical entity that is characterized by angiomatous papules on the extremities. We report a case APACHE in a 14-year-old Japanese girl with asymptomatic red and violaceous papules and nodules on the ring finger of the left hand. Histological and immunohistochemical studies of our patient indicated that APACHE is a pseudolymphoma rather than an angiokeratoma.

MESH: Adolescence-; Angiokeratoma-immunology; Antigens,-Differentiation,-T-Lymphocyte-analysis; Fingers-pathology; Lichen-Planus-pathology; Lymphoma-immunology; Lymphoma-pathology; Skin-pathology; Skin-Neoplasms-immunology

MESH: *Angiokeratoma-pathology; *Skin-Neoplasms-pathology

TG: Case-Report; Female; Human

PT: JOURNAL-ARTICLE

RN: 0

NM: Antigens,-Differentiation,-T-Lymphocyte

AN: 91222965

UD: 9108


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