Literature DB >> 25263662

Microvenular hemangioma: a clinicopathologic review of 13 cases.

Karl M Napekoski1, Anthony P Fernandez, Steven D Billings.   

Abstract

BACKGROUND: Microvenular hemangioma is an uncommon benign vascular tumor that can potentially be mistaken for malignancy.
METHODS: We reviewed the histopathologic and clinical features of 13 microvenular hemangiomas, which represents the largest series reported to date.
RESULTS: The patients [female (F) = 8 and male (M) = 5] had a mean age of 39 years (range: 16 months-69 years). All presented with a similar history of a new, asymptomatic, stable or slow-growing, red to purple plaque or nodule. The lesions were located on the extremities, chest, back or abdomen. Two patients had multiple lesions. In six, a vascular tumor was not suspected clinically. Histologically, all were composed of a dermal proliferation of thin-walled, often branching, vascular channels dissecting through collagen fibers. The vessels were surrounded by a conspicuous layer of pericytes. Immunohistochemistry showed that all were positive for a vascular marker. Stains for WT-1 were positive in 9 of 10. None of the lesions tested (0/12) were positive for podoplanin or human herpesvirus-8 (HHV-8) (0/9). Follow-up available on six patients showed no recurrences.
CONCLUSION: The histomorphology of microvenular hemangioma frequently raises concern for a malignant vascular lesion, especially Kaposi sarcoma. Identification of characteristic features, particularly the pericyte layer in routinely stained sections or with an SMA immunostain, allows an accurate diagnosis.
© 2014 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  Kaposi sarcoma; immunohistochemistry; microvenular hemangioma; vascular tumor

Mesh:

Year:  2014        PMID: 25263662     DOI: 10.1111/cup.12386

Source DB:  PubMed          Journal:  J Cutan Pathol        ISSN: 0303-6987            Impact factor:   1.587


  2 in total

1.  An unusual lesion on the nose: microvenular hemangioma.

Authors:  A Tulin Mansur; Gulsen Tukenmez Demirci; Eltaf A Ozbal Koc; Semsi Yildiz
Journal:  Dermatol Pract Concept       Date:  2018-01-31

2.  Immunoreactivity of Wilms tumor 1 (WT1) as an additional evidence supporting hemangiomatous rather than inflammatory origin in the etiopathogenesis of angiolymphoid hyperplasia with eosinophilia.

Authors:  Fatma Tokat; Julia S Lehman; Engin Sezer; Emel Dikicioglu Cetin; Umit Ince; Emel Ozturk Durmaz
Journal:  Dermatol Pract Concept       Date:  2018-01-31
  2 in total

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