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Journal of the American Academy of Dermatology
Volume 23, n° 2P1
pages 229-235 (août 1990)
Doi : 10.1016/0190-9622(90)70203-T
accepted : 17 November 1989
Clinical and laboratory studies

Benign lymphangioendothelioma
 

Edward Wilson Jones, FRCP, FRCPath a, R.K. Winkelmann, MD, PhD , b, C.B. Zachary, MD, FRCP a, Ashraf M. Reda, MD b : Visiting Clinician
1 London, England 
2 Rochester, Minnesota, USA 

Reprint requests: R. K. Winkelmann, MD, PhD, Department of Dermatology, Mayo Clinic, 200 First St. SW, Rochester, MN 55905
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We have studied eight cases of an acquired lymphatic endothelial lesion for which we propose the name “benign lymphangioendothelioma.” The lesions developed as solitary, slowly extending, erythematous macules and plaques, usually occurring on the extremities or the shoulders in adolescents or adults. The characteristic histopathologic feature is permeation of the dermal collagen by flattened, endothelium-lined channels and spaces. Hemorrhage, iron deposition, and inflammation were not part of the lesion. Ulex europaeus agglutinin I labeled the lesional endothelial cells consistently, but factor VHI-related antigen labeling was negative. This histologic pattern and the special studies suggested a lymphatic lesion. Surgical excision, performed in six patients, was not followed by recurrence.

The full text of this article is available in PDF format.

 Presented at the annual meeting of the North American Clinical Dermatologie Society, Stockholm, Sweden, June 2–9, 1990.

a  From the Institute of Dermatology, St. John's Hospital for Diseases of the Skin, London
b  From the Department of Dermatology, Mayo Clinic and Mayo Foundation, Rochester.

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