| Literature DB >> 19363610 |
Hideki Nakamura1, Junko Kita, Atsushi Kawakami, Satoshi Yamasaki, Hiroaki Ida, Noriho Sakamoto, Akira Furusu, Katsumi Eguchi.
Abstract
Abstract A 66-year-old woman showing renal dysfunction with elevated serum alkaline phosphatase and anti-SS-A antibody was admitted. A labial salivary gland biopsy showing infiltration of mononuclear cells and positive anti-SS-A antibody with sicca symptoms led to a diagnosis of primary Sjögren’s syndrome (SS). Fanconi’s syndrome was diagnosed by renal tubular acidosis along with renal glucosuria or aminoaciduria and multiple bone fractures on bone scintigraphy. Typical bilateral pulmonary shadows were confirmed as organizing pneumonia (OP) determined by the analysis of bronchoalveolar lavage fluid and transbronchial lung biopsy. A rare complication of Fanconi’s syndrome with OP in SS is described.Entities:
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Year: 2009 PMID: 19363610 DOI: 10.1007/s00296-009-0924-5
Source DB: PubMed Journal: Rheumatol Int ISSN: 0172-8172 Impact factor: 2.631