Anaplastic Large B-Cell Lymphoma: Cutaneous Presentations

Anaplastic large cell lymphoma (ALCL) is a rare T-cell lymphoma characterized by CD30 expression. This report describes the case of a 10-year-old female who presented with non-resolving cutaneous lesions initially treated as a bacterial infection. A biopsy confirmed the diagnosis of anaplastic lymphoma kinase-negative (ALK-negative) ALCL with cutaneous and nodal involvement. Further imaging revealed neoplastic uptake in the right lung, and the patient was diagnosed with Murphy stage II ALCL. She began chemotherapy according to established pediatric oncology protocols. ALCL presents diagnostic challenges due to its non-specific symptoms, which can mimic benign conditions. This case underscores the importance of early biopsy and molecular testing when standard treatments fail. Early recognition and routine examinations, including lymph node assessments and skin biopsies, are critical for improving patient outcomes, as timely diagnosis leads to more effective treatment options and potential remission.

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Publication Details

Journal
Cureus
Published
2024-10-14
DOI
https://doi.org/10.7759/cureus.71430
Primary Topic
Cutaneous lymphoproliferative disorders research
Type
article
Field-Weighted Citation Impact
0.00
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article

Anaplastic Large B-Cell Lymphoma: Cutaneous Presentations

Ian Depew, William T Snider, Shane Cook
Cureus
Cutaneous lymphoproliferative disorders research
article

Anaplastic Large B-Cell Lymphoma: Cutaneous Presentations

Ian Depew, William T Snider, Shane Cook
article en

Abstract

Anaplastic large cell lymphoma (ALCL) is a rare T-cell lymphoma characterized by CD30 expression. This report describes the case of a 10-year-old female who presented with non-resolving cutaneous lesions initially treated as a bacterial infection. A biopsy confirmed the diagnosis of anaplastic lymphoma kinase-negative (ALK-negative) ALCL with cutaneous and nodal involvement. Further imaging revealed neoplastic uptake in the right lung, and the patient was diagnosed with Murphy stage II ALCL. She began chemotherapy according to established pediatric oncology protocols. ALCL presents diagnostic challenges due to its non-specific symptoms, which can mimic benign conditions. This case underscores the importance of early biopsy and molecular testing when standard treatments fail. Early recognition and routine examinations, including lymph node assessments and skin biopsies, are critical for improving patient outcomes, as timely diagnosis leads to more effective treatment options and potential remission.

CureusVol. 16(10)
Marshall University (US)
Zero hunger
Openalex Percentile: Top 63%
Cutaneous lymphoproliferative disorders research
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