Cutaneous Eruptions as a Consequence of Myeloid Leukemic Infiltration: Differential Diagnosis With a Benign Dermatosis

Leukemia cutis is an uncommon but clinically significant manifestation of hematologic malignancies caused by infiltration of the skin by malignant leukocytes. Its presentation is highly variable and may closely resemble benign inflammatory dermatoses, frequently leading to diagnostic delay. We report the case of a 76-year-old man with JAK2-positive essential thrombocythemia (ET) who developed persistent, intensely pruritic maculopapular skin lesions initially diagnosed as dermatitis. Despite symptomatic treatment, the lesions progressed and were followed by systemic symptoms. Further investigation revealed acute myeloid leukemia (AML) arising from blastic transformation of ET, with probable cutaneous involvement consistent with leukemia cutis. This case highlights the importance of maintaining a high index of suspicion when evaluating new or treatment-refractory skin lesions in patients with myeloproliferative neoplasms (MPNs), as early recognition may allow timely diagnosis of leukemic transformation and prompt initiation of appropriate therapy.

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Publication Details

Journal
Cureus
Published
2026-01-03
DOI
https://doi.org/10.7759/cureus.100672
Primary Topic
Myeloproliferative Neoplasms: Diagnosis and Treatment
Type
article
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article

Cutaneous Eruptions as a Consequence of Myeloid Leukemic Infiltration: Differential Diagnosis With a Benign Dermatosis

Ricardo C Martins, Tiago S Duarte, Cristiana L Matos
Cureus
Myeloproliferative Neoplasms: Diagnosis and Treatment
article

Cutaneous Eruptions as a Consequence of Myeloid Leukemic Infiltration: Differential Diagnosis With a Benign Dermatosis

Ricardo C Martins, Tiago S Duarte, Cristiana L Matos
article en

Abstract

Leukemia cutis is an uncommon but clinically significant manifestation of hematologic malignancies caused by infiltration of the skin by malignant leukocytes. Its presentation is highly variable and may closely resemble benign inflammatory dermatoses, frequently leading to diagnostic delay. We report the case of a 76-year-old man with JAK2-positive essential thrombocythemia (ET) who developed persistent, intensely pruritic maculopapular skin lesions initially diagnosed as dermatitis. Despite symptomatic treatment, the lesions progressed and were followed by systemic symptoms. Further investigation revealed acute myeloid leukemia (AML) arising from blastic transformation of ET, with probable cutaneous involvement consistent with leukemia cutis. This case highlights the importance of maintaining a high index of suspicion when evaluating new or treatment-refractory skin lesions in patients with myeloproliferative neoplasms (MPNs), as early recognition may allow timely diagnosis of leukemic transformation and prompt initiation of appropriate therapy.

CureusVol. 18(1)
Administração Regional de Saúde de Lisboa e Vale do Tejo (PT)
Good health and well-being
Openalex Percentile: Top 98%
Myeloproliferative Neoplasms: Diagnosis and Treatment
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