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Updated: Jul 21, 2025

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Granulocyte-dependent Autoantibody-induced Skin Blistering
Published on: October 12, 2012
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Blistering and aggressive paniculite cutaneous T-cell lymphoma.
Eduardo Marín-Hernández1, Angélica D De-Las-Fuentes-García2, Georgina A Siordia-Reyes3
1Servicio de Dermatología Pediátrica, Unidad Médica de Alta Especialidad, Hospital de Pediatría, Centro Médico Nacional Siglo XXI, Instituto Mexicano del Seguro Social.
Boletin Medico Del Hospital Infantil De Mexico
|July 25, 2023
Summary
Subcutaneous panniculitis-like T-cell lymphoma (SPTCL) is a rare T-cell lymphoma. This case highlights SPTCL in a child, emphasizing diagnostic challenges and the importance of early recognition for improved outcomes.
Area of Science:
- Dermatology
- Hematology
- Pediatric Oncology
Background:
- Subcutaneous panniculitis-like T-cell lymphoma (SPTCL) is a rare neoplastic proliferation of atypical T-cells in the subcutaneous fat.
- While typically indolent and affecting middle-aged adults, SPTCL can present aggressively and rarely occur in children.
Observation:
- A previously healthy 12-year-old male presented with a disseminated dermatosis.
- Clinical manifestations included vesicles, blisters, erythematous and hematonecrotic plaques, atrophic scars, and edema.
Findings:
- Histopathological examination confirmed limited cutaneous SPTCL with extensive epidermal necrosis.
- This case represents a rare pediatric presentation of SPTCL.
Implications:
- The diagnosis of SPTCL should be considered in children with similar clinical presentations, especially those refractory to initial treatments.
- Timely diagnosis and appropriate management are crucial for improving patient survival in pediatric SPTCL.
- This case underscores the need for increased awareness of SPTCL in pediatric dermatology and oncology.
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