Pyoderma gangrenosum in a newborn - case report

Author:

Carneiro Francisca Regina Oliveira1,Santos Maria Amélia Lopes dos2,Sousa Brena Andrade de3,Nascimento Carla do Socorro Silva do3,Amin Gabriela Athayde3,Moutinho Ana Thais Machado3

Affiliation:

1. São Paulo Federal University; Pará State University, Brazil

2. Pará State University; Pará State University, Brazil

3. Pará State University, Brazil

Abstract

Pyoderma gangrenosum is a rare, inflammatory, chronic and recurrent disease of unknown etiology, characterized by noninfectious, necrotizing and painful cutaneous ulcers. Usually it affects adults aged between 25 and 54 years old and rarely children (less than 4%), in which it mainly affects the head, face, buttocks, genital and perianal region. The disease presents a quick response to systemic corticosteroids. We report a case of a newborn with hemorrhagic and necrotic ulcers, distributed in the abdomen, buttocks and genital region with rapid and effective response to oral prednisone.

Publisher

FapUNIFESP (SciELO)

Subject

Dermatology

Reference10 articles.

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4. Pyoderma gangrenosum: an Indian perspective;Bhat RM;Clin Exp Dermatol,2011

5. Bullous pyoderma gangrenosum and myelodysplastic syndrome;Batista MD;An Bras Dermatol,2006

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1. A repair of the oral commissure performed on scars due to pyoderma gangrenosum in a girl;Japanese Journal of Oral and Maxillofacial Surgery;2022-06-20

2. A case of pyoderma gangrenosum with oral lesions in an 8-year-old girl;Japanese Journal of Oral and Maxillofacial Surgery;2019-05-20

3. Pyoderma gangrenosum in an infant: A case report and review of the literature;Pediatric Dermatology;2018-04-15

4. Ocular pyoderma gangrenosum: A systematic review;Journal of the American Academy of Dermatology;2017-03

5. Cutaneous Manifestations of Systemic Disease;Therapy in Pediatric Dermatology;2016-12-17

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