Pyoderma Gangrenosum in a Patient With Hereditary Spherocytosis
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kwon, Hyoung Il | - |
dc.contributor.author | Paek, Jun Oh | - |
dc.contributor.author | Kim, Jeoung Eun | - |
dc.contributor.author | Ro, Young Suck | - |
dc.contributor.author | Ko, Joo Yeon | - |
dc.date.accessioned | 2022-07-15T18:11:36Z | - |
dc.date.available | 2022-07-15T18:11:36Z | - |
dc.date.created | 2021-05-12 | - |
dc.date.issued | 2016-03 | - |
dc.identifier.issn | 1534-7346 | - |
dc.identifier.uri | https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/155011 | - |
dc.description.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. | - |
dc.language | 영어 | - |
dc.language.iso | en | - |
dc.publisher | SAGE PUBLICATIONS INC | - |
dc.title | Pyoderma Gangrenosum in a Patient With Hereditary Spherocytosis | - |
dc.type | Article | - |
dc.contributor.affiliatedAuthor | Kim, Jeoung Eun | - |
dc.contributor.affiliatedAuthor | Ro, Young Suck | - |
dc.contributor.affiliatedAuthor | Ko, Joo Yeon | - |
dc.identifier.doi | 10.1177/1534734615623432 | - |
dc.identifier.scopusid | 2-s2.0-84959502053 | - |
dc.identifier.wosid | 000371697400018 | - |
dc.identifier.bibliographicCitation | INTERNATIONAL JOURNAL OF LOWER EXTREMITY WOUNDS, v.15, no.1, pp.92 - 95 | - |
dc.relation.isPartOf | INTERNATIONAL JOURNAL OF LOWER EXTREMITY WOUNDS | - |
dc.citation.title | INTERNATIONAL JOURNAL OF LOWER EXTREMITY WOUNDS | - |
dc.citation.volume | 15 | - |
dc.citation.number | 1 | - |
dc.citation.startPage | 92 | - |
dc.citation.endPage | 95 | - |
dc.type.rims | ART | - |
dc.type.docType | Article | - |
dc.description.journalClass | 1 | - |
dc.description.isOpenAccess | N | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Dermatology | - |
dc.relation.journalResearchArea | Surgery | - |
dc.relation.journalWebOfScienceCategory | Dermatology | - |
dc.relation.journalWebOfScienceCategory | Surgery | - |
dc.subject.keywordPlus | ANEMIA | - |
dc.subject.keywordAuthor | hereditary spherocytosis | - |
dc.subject.keywordAuthor | leg | - |
dc.subject.keywordAuthor | pyoderma gangrenosum | - |
dc.subject.keywordAuthor | ulcers | - |
dc.identifier.url | https://journals.sagepub.com/doi/10.1177/1534734615623432 | - |
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