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CC BY-NC-ND 4.0 · Indian J Med Paediatr Oncol 2018; 39(02): 247-249
DOI: 10.4103/ijmpo.ijmpo_74_17
Case Report

Xeroderma Pigmentosum and Bone Marrow Aplasia: A Rare Association

Sakthisankari Shanmugasundaram
Department of Pathology, PSG Institute of Medical Sciences and Research, Coimbatore, Tamil Nadu, India
,
Prasanna N Kumar
Department of Pathology, PSG Institute of Medical Sciences and Research, Coimbatore, Tamil Nadu, India
,
S Vidhya Lakshmi
Department of Pathology, PSG Institute of Medical Sciences and Research, Coimbatore, Tamil Nadu, India
,
V Chaitra
Department of Pathology, PSG Institute of Medical Sciences and Research, Coimbatore, Tamil Nadu, India
› Institutsangaben Financial support and sponsorship Nil.
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Abstract

Xeroderma pigmentosum (XP) is a rare autosomal recessive disorder characterized by hypersensitivity to ultraviolet rays and predisposition to cutaneous malignancies. Hematological disorders associated with XP include myelodysplastic syndrome and acute leukemia. We report a 7-year-old child with XP along with squamous cell carcinoma and bone marrow aplasia.

Keywords

Aplastic anemia - pancytopenia - squamous cell carcinoma - xeroderma pigmentosum


Publikationsverlauf

Artikel online veröffentlicht:
23. Juni 2021

© 2018. Indian Society of Medical and Paediatric Oncology. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial-License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/.)

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