Lymphomatoid Papulosis Type D: Report of a Case in a Child and Review of the Literature
Author:
Affiliation:
1. Department of Pathology; School of Medicine and Dentistry; University of Rochester; Rochester New York
2. Department of Dermatology; School of Medicine and Dentistry; University of Rochester; Rochester New York
Publisher
Wiley
Subject
Dermatology,Pediatrics, Perinatology and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/pde.12743/fullpdf
Reference16 articles.
1. Lymphomatoid papulosis. A continuing self-healing eruption, clinically benign-histologically malignant;Macaulay;Arch Dermatol,1968
2. Clinical, histopathologic, and immunophenotypic features of lymphomatoid papulosis with CD8 predominance in 14 pediatric patients;De Souza;J Am Acad Dermatol,2009
3. WHO-EORTC classification for cutaneous lymphomas;Willemze;Blood,2005
4. A variant of lymphomatoid papulosis simulating primary cutaneous aggressive epidermotropic CD8+ cytotoxic T-cell lymphoma. Description of 9 cases;Saggini;Am J Surg Pathol,2010
5. The differential diagnosis of CD8-positive (“type D”) lymphomatoid papulosis;McQuitty;J Cutan Pathol,2014
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1. Type D lymphomatoid papulosis with pityriasis lichenoides et varioliformis acuta-like features in a child with parvovirus infection: a controversial diagnosis in the spectrum of lymphoid proliferations: case report and literature review;Italian Journal of Pediatrics;2022-10-28
2. Childhood lymphomatoid papulosis Type D, a rare and challenging diagnosis;Pediatric Dermatology;2022-07-11
3. Lymphomatoid papulosis types D and E: a multicentre series of the French Cutaneous Lymphomas Study Group;Clinical and Experimental Dermatology;2021-07-28
4. Lymphomatoid Papulosis;Diagnostic Pathology: Neoplastic Dermatopathology;2017
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