This Article  • References  • Full text PDF  • Send to a friend  • Save in My Folder  • Save to citation manager  • Permissions  Citing Articles  • Citation map  • Citing articles on HighWire  • Contact me when this article is cited  Related Content  • Similar articles in this journal  Social Bookmarking   What's this?

Philip H. Cooper, MD; Henry F. Frierson, MD; Allan L. Kayne, MD; Hernan Sabio, MD

Arch Dermatol. 1984;120(3):371-375.

Abstract
• Multiple cutaneous xanthomas developed in a patient at the age of 10 months, and juvenile chronic myeloid leukemia (JCML) developed at the age of 30 months. The xanthomas were histopathologically consistent with a diagnosis of juvenile xanthogranuloma (JXG). A review of other cases of JCML with JXG indicates that the cutaneous lesions have many clinical and histopathologic similarities to sporadic JXG but are more often multiple or papular and confluent. In addition to JXG, a few children with JCML also have multiple café-au-lait spots and a family history of neurofibromatosis.

(Arch Dermatol 1984;120:371-375)

Author Affiliations
From the Departments of Pathology (Drs Cooper and Frierson), Dermatology (Drs Cooper and Kayne), and Pediatrics (Dr Sabio), University of Virginia, Charlottesville.

Footnotes
Accepted for publication Nov 22, 1982.

Reprint requests to Department of Pathology, Box 214, University of Virginia Medical Center, Charlottesville, VA 22908 (Dr Cooper).

CiteULike    Connotea    Del.icio.us    Digg    Reddit    Technorati    Twitter     What's this?

THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Red Eroded Nodule on the Foot
Cornelius and Wilson
Arch Dermatol 1999;135:707-712.
FULL TEXT  

Juvenile Xanthogranuloma, Neurofibromatosis, and Juvenile Chronic Myelogenous Leukemia: World Statistical Analysis
Zvulunov et al.
Arch Dermatol 1995;131:904-908.
ABSTRACT  

Primary Histiocytic Dermatoses
Ringel and Moschella
Arch Dermatol 1985;121:1531-1541.
ABSTRACT