A Case of Nonvenereal Sclerosing Lymphangitis of the Penis.
10.5021/ad.1999.11.4.236
- Author:
Hyohyun AHN
;
Aeri KIM
;
Il Hwan KIM
- Publication Type:Case Report
- Keywords:
Sclerosing lymphangitis;
Penis;
Factor VIII related antigen;
CD-34
- MeSH:
Adult;
Biopsy;
Humans;
Hypertrophy;
Lymphangitis*;
Lymphatic Vessels;
Male;
Penis*;
Sclerosis;
von Willebrand Factor
- From:Annals of Dermatology
1999;11(4):236-239
- CountryRepublic of Korea
- Language:English
-
Abstract:
The patient was a 41-year-old healthy man, who developed a tender, cord-like serpiginous mass just proximal to the coronal sulcus for two weeks. He was a sexually active, non-promiscuous, married man. We had taken a biopsy, and noticed the subsiding of the lesion without further treatment. Nonvenereal sclerosing lymphangitis of the penis is a rare self-limiting peculiar disorder involving the lymphatics of the penile sulcus. Clinically, it presents as a cord-like nodular penile lesion with characteristic cartilaginous firmness. Histologically, it is described as hypertrophy and sclerosis of the lymphatic vessel walls with mild inflammatory cellular infiltration, and occasional obstruction of the lymphatic vessel. But, because such features including sclerosis varies according to the time when the biopsy was taken, they are not attributable to all cases. Our case shows the same clinical and pathological features of ‘benign transient lymphangiectasis’. Except for the painful cases, no specific treatments are usually warranted.
