Pancreatic Panniculitis in an 18-Month-Old with Complete DiGeorge Syndrome.
Citation: Pediatric Dermatology. 33(3):e206-7, 2016 MayPMID: 27040037Institution: MedStar Washington Hospital CenterDepartment: DermatologyForm of publication: Journal ArticleMedline article type(s): Journal ArticleSubject headings: *DiGeorge Syndrome/di [Diagnosis] | *Pancreatitis/di [Diagnosis] | *Panniculitis/di [Diagnosis] | *Skin/pa [Pathology] | Acute Disease | Biopsy, Needle | DiGeorge Syndrome/co [Complications] | Disease Progression | Fatal Outcome | Humans | Immunohistochemistry | Infant | Lower Extremity | Male | Pancreatitis/co [Complications] | Panniculitis/co [Complications]Year: 2016ISSN:- 0736-8046
Item type | Current library | Collection | Call number | Status | Date due | Barcode |
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Journal Article | MedStar Authors Catalog | Article | 27040037 | Available | 27040037 |
Copyright � 2016 Wiley Periodicals, Inc.
Pancreatic panniculitis, characterized by tender, erythematous subcutaneous nodules occurring most commonly on the lower extremities, occurs in 2% of cases of pancreatic disease. We present a rare case of pancreatic panniculitis in a child with complete DiGeorge syndrome.
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