Xeroderma Pigmentosum and Bone Marrow Aplasia: A Rare Association

Author:

Shanmugasundaram Sakthisankari1,Kumar Prasanna N1,Lakshmi S Vidhya1,Chaitra V1

Affiliation:

1. Department of Pathology, PSG Institute of Medical Sciences and Research, Coimbatore, Tamil Nadu, India

Abstract

AbstractXeroderma 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.

Publisher

Georg Thieme Verlag KG

Subject

Oncology,Pediatrics, Perinatology and Child Health

Reference10 articles.

1. Xeroderma pigmentosa - A rare clinical entity;A K Bilodi;Indian J Med Case Rep,2013

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3. Clinical profile and mutation analysis of xeroderma pigmentosum in Indian patients;P M Tamhankar;Indian J Dermatol Venereol Leprol,2015

4. Xeroderma pigmentosa with ocular association: Case report;A Pandey;Case Rep Clin Med,2013

5. Xeroderma pigmentosum – A case report with oral implications;C Lopes-Cardoso;J Clin Exp Dent,2012

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