Literature DB >> 6863623

Acquired progressive lymphangioma.

M Watanabe, K Kishiyama, A Ohkawara.   

Abstract

A 5-year-old Japanese boy, who developed dark brown, erythematous lesions (two separate lesions) on his face, scalp, and left upper arm within 2 years, was reported. Biopsy specimens revealed many dilated channels lined by a single layer of endothelial cells without obvious atypicality throughout the dermis. These channels split collagen bundles, giving a "dissection of collagen" appearance. From these clinical and histopathologic findings, we have diagnosed these lesions as acquired progressive lymphangioma. Our patient is the youngest reported patient in the literature, and we were interested in that the two lesions developed separately following previous trauma and they had the tendency to regress following oral prednisolone therapy.

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Year:  1983        PMID: 6863623     DOI: 10.1016/s0190-9622(83)70076-9

Source DB:  PubMed          Journal:  J Am Acad Dermatol        ISSN: 0190-9622            Impact factor:   11.527


  2 in total

1.  Benign Lymphangioendothelioma - A Case Report.

Authors:  Naveen Kumar Vittal; Sushruth Guruputra Kamoji; Shilpa Vinay Dastikop
Journal:  J Clin Diagn Res       Date:  2016-01-01

2.  Benign Lymphangioendothelioma: A Report of a Rare Vascular Hamartoma in a Young Indian Child.

Authors:  Olympia Rudra; Arghyaprasun Ghosh; Sudip Kumar Ghosh; Deblina Bhunia; Prabhakar Mandal
Journal:  Indian J Dermatol       Date:  2017 Sep-Oct       Impact factor: 1.494

  2 in total

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