Evidence map›Paper›PMID 42464172›Full record

ArticleBMC pediatrics2026

Leukemia cutis of the scalp as a first manifestation of B-cell lymphoblastic leukemia: an unusual presentation.

Bahareh Abtahi-Naeini, Zahra Pourmoghaddas, Maryam Derakhshan, Alireza Moafi, Fateme Ahmadinia, Elaheh Foroughi

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Article in BMC pediatrics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Bahareh Abtahi-NaeiniSkin Diseases and Leishmaniasis Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.
Zahra PourmoghaddasDepartment of Pediatrics, Isfahan University of Medical Sciences, Isfahan, Iran.
Maryam DerakhshanDepartment of Pathology, Isfahan University of Medical Sciences, Isfahan, Iran.
Alireza MoafiDepartment of Pediatric Hematology and Oncology, Isfahan University of Medical Sciences, Isfahan, Iran.
Fateme AhmadiniaStudent research committee, Isfahan University of Medical Sciences, Isfahan, Iran. fatemeahmadinia1313@gmail.com.
Elaheh ForoughiStudent research committee, Isfahan University of Medical Sciences, Isfahan, Iran. elahehforoughi2002@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLeukemia cutis (LC) is an extramedullary manifestation of leukemia that occurs when neoplastic cells infiltrate the epidermis, dermis, or subcutaneous tissue of the skin. The clinical presentation of LC can vary significantly and is typically a late sign in advanced disease. In this case report, we describe a diagnostically challenging case of LC in a 10-year-old girl who initially presented with a solitary morphea-like plaque on her scalp, which ultimately led to the diagnosis of B-cell acute lymphoblastic leukemia (B-cell ALL). CASE PRESENTATION: We present a challenging case of a 10-year-old female who initially presented with a scarring alopecic, morphea-like plaque on the right parietal scalp. Over two months, the lesion proved unresponsive to high-dose topical corticosteroid therapy and demonstrated progressive enlargement. The clinical course was further complicated by the emergence of systemic symptoms, including recurrent fever and significant cervical lymphadenopathy, which prompted referral for further evaluation. A definitive diagnosis of B-cell ALL was established based on congruent histopathological and immunohistochemical profiles from biopsies of the scalp lesion and cervical lymph nodes, which were confirmed by bone marrow examination. The patient achieved complete remission of the cutaneous lesion and systemic disease following one month of chemotherapy according to the Berlin-Frankfurt-Münster (BFM) protocol.

conclusionGiven the highly variable clinical presentations of leukemia cutis, this case highlights the critical necessity of including it in the differential diagnosis of atypical sclerotic scalp lesions in children. A strong clinical suspicion is required for the timely diagnosis of uncommon cutaneous presentations of underlying hematologic malignancy. Appropriate biopsy and the prompt initiation of systemic chemotherapy are paramount for achieving favorable outcomes and remission.

Indexed as

Leukemic InfiltrationPrecursor B-Cell Lymphoblastic Leukemia-LymphomaScalpSkin NeoplasmsChildDiagnosis, DifferentialFemaleHumansPrecursor Cell Lymphoblastic Leukemia-LymphomaB-Cell acute lymphoblastic leukemiaB-cell ALLLeukemia cutis

Identifiers

PMID42464172
PMCPMC13663134

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