Pyoderma Gangrenosum in a Patient With Hereditary Spherocytosis
- Authors
- Kwon, Hyoung Il; Paek, Jun Oh; Kim, Jeoung Eun; Ro, Young Suck; Ko, Joo Yeon
- Issue Date
- Mar-2016
- Publisher
- SAGE PUBLICATIONS INC
- Keywords
- hereditary spherocytosis; leg; pyoderma gangrenosum; ulcers
- Citation
- INTERNATIONAL JOURNAL OF LOWER EXTREMITY WOUNDS, v.15, no.1, pp.92 - 95
- Indexed
- SCIE
SCOPUS
- Journal Title
- INTERNATIONAL JOURNAL OF LOWER EXTREMITY WOUNDS
- Volume
- 15
- Number
- 1
- Start Page
- 92
- End Page
- 95
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/155011
- DOI
- 10.1177/1534734615623432
- ISSN
- 1534-7346
- Abstract
- Pyoderma gangrenosum (PG) is a rare, relapsing cutaneous disease with 4 distinctive clinical manifestations: ulcerative, bullous, pustular, and vegetative lesions. It mainly occurs in adults and is frequently associated with systemic diseases, most commonly inflammatory bowel disease, rheumatologic disease, or hematological dyscrasias. However, there have been no previous reports of PG in a patient with hereditary spherocytosis, a common inherited hemolytic anemia. We report here a unique case of PG in a 15-year-old boy with underlying hereditary spherocytosis.
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