Pyoderma Gangrenosum in a Patient With Hereditary Spherocytosis.
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...
| Publicado en: | International Journal of Lower Extremity Wounds Vol. 15; no. 1; pp. 92 - 96 |
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| Autores principales: | , , , , |
| Formato: | case study pictorial tables/charts Journal Article |
| Publicado: |
Sage Publications Inc.
Mar2016
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| Acceso en línea: | Ver este registro en EBSCOhost |
| fields | @attributes: recordID: 1 pdfLink: plink: https://search.ebscohost.com/login.aspx?direct=true&db=ccm&AN=113451424&site=ehost-live header: @attributes: shortDbName: ccm uiTerm: 113451424 longDbName: CINAHL Complete uiTag: AN controlInfo: bkinfo: dissinfo: jinfo: jid: 15347346 IYG jtl: International Journal of Lower Extremity Wounds issn: 15347346 maglogo: Y pubinfo: dt: Mar2016 vid: 15 iid: 1 pid: 344 pub: Sage Publications Inc. place: Thousand Oaks, California artinfo: ui: 113451424 113451424 113451424 10.1177/1534734615623432 113451424 ppf: 92 ppct: 4 formats: tig: atl: Pyoderma Gangrenosum in a Patient With Hereditary Spherocytosis. aug: au: Kwon, Hyoung Il Paek, Jun Oh Kim, Jeoung Eun Ro, Young Suck Ko, Joo Yeon affil: Hanyang University Hospital, Hanyang University College of Medicine, Seoul, Korea sug: subj: Anemia, Hemolytic, Congenital Familial and Genetic Anemia, Hemolytic, Congenital Complications Pyoderma Gangrenosum Etiology Adolescence Male Adolescent: 13-18 years Male ab: 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. pubtype: Academic Journal doctype: case study pictorial tables/charts Journal Article ougenre: Article language: English refInfo: holdings: @attributes: islocal: N |
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