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Aleukemia Cutis: Clinicopathological and Molecular Investigation of Two Cases Publisher Pubmed



Azariyaam A1 ; Safavi M1 ; Ghanadan A2
Authors
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Authors Affiliations
  1. 1. Molecular Pathology and Cytogenetics Division, Department of Pathology, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran
  2. 2. Department of Pathology, Imam Khomeini Hospital, Tehran University of Medical Sciences, Tehran, Iran

Source: Journal of Cutaneous Pathology Published:2020


Abstract

We describe two cases of acute myeloid leukemia (AML) who presented with cutaneous manifestations. Leukemia cutis (LC) is the cutaneous presentation of any type of leukemia and occurs in 10% to 15% of patients with AML, but cutaneous infiltration of AML rarely precedes the involvement of the bone marrow or peripheral blood and is called “aleukemia cutis.” Our first case presented with facial skin thickening, a manifestation which is known as lionization and his initial clinical diagnosis was nonspecific allergic reaction. Our second case presented with urticaria-like lesions with the initial clinical and histomorphologic diagnoses of leukocytoclastic vasculitis. Histopathologic examination of skin biopsy specimens in both patients showed diffuse infiltration of the dermis with a monotonous population of intermediate-sized mononuclear cells by open chromatin and promonocytic features. Bone marrow aspiration leukocyte karyotyping showed normal cytogenetics, and molecular investigation revealed mutations of NPM1 and FLT3 genes. Somatic CEBPA gene mutation was negative in both patients. LC as the first manifestation of leukemia is very rare and could result in delayed diagnosis and affect patient prognosis. © 2020 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.