
Leg Ulcers in Mediterranean AnemiaA Report of Two New Cases in Sisters
M. H. SAMITZ, MD;
DONALD S. WALDORF, MD;
JOSEPH SHRAGER, MD
Arch Dermatol. 1964;90(6):567-571.
Abstract
Two additional patients with thalassemia minor and ankle ulcers are reported, bringing the total number reported to ten.
A genealogic study of the thalassemic trait in their family was traced. From a review of the literature it appears that all previous patients with thalassemia and leg ulcers had thalassemia minor. The composite affected patient is a 26-year-old Italian-decended woman with splenomegaly and a hemoglobin of about 8 gm/100 ml.
The pathogenesis of the ulcers is nonspecific.
Treatment is that of a stasis ulcer.
Author Affiliations
PHILADELPHIA
From the Department of Dermatology, School of Medicine, University of Pennsylvania.
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