Literature DB >> 10935645

Benign lymphangioendothelioma (acquired progressive lymphangioma): a lesion not to be confused with well-differentiated angiosarcoma and patch stage Kaposi's sarcoma: clinicopathologic analysis of a series.

L Guillou1, C D Fletcher.   

Abstract

The clinicopathologic features of 12 cases of benign lymphangioendothelioma (acquired progressive lymphangioma) are reported. There were five male and seven female patients. Age at diagnosis ranged from 17 to 90 years (median age, 54 yrs). Development of a single macular/papular hemangiomatous or pigmented lesion was the main presenting symptom. Symptom duration before diagnosis ranged from 2 months to 20 years (median, 5.5 yrs). Tumor size ranged from 0.3 cm to 10 cm (median. 1.5 cm). Location included skin of the head and neck (n = 5), back (n = 1), breast (n = 1), shoulder (n = 1), forearm (n = 1), plantar aspect of the foot (n = 2), and oral mucosa (n = 1). No patient had any other concomitant vascular anomaly (for example, lymphangiomatosis) or was suspected to have acquired immunodeficiency syndrome. Treatment consisted of excisional biopsy in nine patients, incisional biopsy in two, and wide excision in one. Follow-up information on nine patients (range, 4-40 mos; median, 12 mos) showed two local recurrences in one patient. Microscopically, the lesions consisted of anastomosing, often widely dilated vascular structures developing in the superficial dermis. As the lesion grew within deeper dermis, the vascular spaces collapsed and dissected the dermal collagen in an angiosarcoma-like pattern. The lining endothelium was flat and monolayered, with little or no cytologic atypia and no evident mitoses. Some vascular structures contained stromal papillary projections resembling papillary endothelial hyperplasia, and intravascular red blood cells were present occasionally. Immunohistochemistry performed in eight specimens showed variable endothelial cell reactivity for CD31 (7 of 8), CD34 (7 of 7), and factor VIII-related antigen (4 of 6). A smooth muscle cell layer was observed focally around the vascular spaces in six lesions. Benign lymphangioendothelioma (acquired progressive lymphangioma) is an uncommon benign lesion that, in view of major differences in treatment and prognosis, should be distinguished from well-differentiated angiosarcoma and Kaposi's sarcoma, especially the patch stage and lymphangioma-like variants of the latter.

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Year:  2000        PMID: 10935645     DOI: 10.1097/00000478-200008000-00002

Source DB:  PubMed          Journal:  Am J Surg Pathol        ISSN: 0147-5185            Impact factor:   6.394


  7 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.  Acquired progressive lymphangioma of the nipple.

Authors:  Eyas Alkhalili; Houriya Ayoubieh; William O'Brien; Steven D Billings
Journal:  BMJ Case Rep       Date:  2014-09-22

3.  Post-mastectomy benign lymphangioendothelioma of the skin following chronic lymphedema for breast carcinoma: a teaching case mimicking low-grade angiosarcoma and masquerading as Stewart-Treves syndrome.

Authors:  Sohsuke Yamada; Yoko Yamada; Miwa Kobayashi; Ryosuke Hino; Aya Nawata; Hirotsugu Noguchi; Motonobu Nakamura; Toshiyuki Nakayama
Journal:  Diagn Pathol       Date:  2014-10-29       Impact factor: 2.644

4.  Immunocompromised Districts of Skin: A Case Series and a Literature Review.

Authors:  Aleksandra Vojvodic; Michael Tirant; Veronica di Nardo; Torello Lotti; Uwe Wollina
Journal:  Open Access Maced J Med Sci       Date:  2019-09-10

5.  Histological variants of cutaneous Kaposi sarcoma.

Authors:  Wayne Grayson; Liron Pantanowitz
Journal:  Diagn Pathol       Date:  2008-07-25       Impact factor: 2.644

6.  A Case of Patch Stage of Kaposi's Sarcoma and Discussion of the Differential Diagnosis.

Authors:  Ipshita Kak; Samih Salama; Gabriella Gohla; Asghar Naqvi; Salem Alowami
Journal:  Rare Tumors       Date:  2016-03-31

7.  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

  7 in total

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