A rare case of late myelodysplasia cutis associated with essential thrombocythemia: A case report-Reference-Cited by-同舟云学术

A rare case of late myelodysplasia cutis associated with essential thrombocythemia: A case report

Published:2022-01 Issue: Volume:10 Page:2050313X2210857
ISSN:2050-313X
Container-title:SAGE Open Medical Case Reports
language:en
Short-container-title:SAGE Open Medical Case Reports

Author:

Fournier Suzel¹^ORCID,Mailhot Sylvain²,Bujold Janie³

Affiliation:

1. CHU de Québec—Université Laval, Québec, QC, Canada

2. CHU Dr-Georges-L.-Dumont—PathAssistant Laboratory, Moncton, NB, Canada

3. CISSS de la Gaspésie—Hôpital de Maria, Maria, QC, Canada

Abstract

Myelodysplasia cutis is a relatively new described entity that is characterized by cutaneous plaques and nodules representing dermal infiltration of myeloid immature non-blastic cells. It can be related to myelodysplastic syndromes or myeloproliferative disorders. It has distinct clinical and histopathological features in comparison with leukemia cutis. We report an unusual case of late myelodysplasia cutis in a male patient with essential thrombocythemia. It is only the second case reported to be related to this myeloproliferative disorder.

Publisher

SAGE Publications

Subject

General Medicine

Link

http://journals.sagepub.com/doi/pdf/10.1177/2050313X221085760

Reference5 articles.

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3. Myelodysplasia Cutis Versus Leukemia Cutis

4. Myelodysplasia cutis associée à un syndrome myéloprolifératif

5. Identification of clonal skin myeloid cells by next‐generation sequencing in myelodysplasia cutis

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1. Myelodysplasia cutis and VEXAS syndrome initially diagnosed as histiocytoid Sweet syndrome: A diagnostic pitfall;Journal of Cutaneous Pathology;2024-07-12

2. Myelodysplasia cutis masquerading as granulomatous dermatitis;Journal of Cutaneous Pathology;2023-12-13

3. Myelodysplasia Cutis;Archives of Pathology & Laboratory Medicine;2023-10-03