| Literature DB >> 26555284 |
Tomotaka Suzuki1,2, Shigeru Kusumoto3, Taro Yamashita4, Arisa Masuda1, Shiori Kinoshita1, Takashi Yoshida1, Fumiko Takami-Mori1,2, Hisashi Takino5, Asahi Ito1, Masaki Ri1, Takashi Ishida1, Hirokazu Komatsu1, Mitsuharu Ueda4, Yukio Ando4, Hiroshi Inagaki5, Shinsuke Iida1.
Abstract
Our goal was to evaluate the usefulness of labial salivary gland (LSG) biopsy for diagnosing immunoglobulin light chain (AL) amyloidosis, by comparing bone marrow and skin biopsies in the same patient population. This retrospective study included 34 consecutive patients who showed evidence of monoclonal proteins and symptoms considered to be due to amyloidosis, and who underwent a tissue biopsy from LSG between January 2005 and December 2012 at Nagoya City University Hospital. All samples of superficial tissues, including LSG, bone marrow, and skin, were independently evaluated as having amyloid deposits by a central review, which was blind to clinical information. An AL amyloidosis diagnosis was based on evidence of amyloid deposition in any biopsied tissue. Eighteen patients were diagnosed with AL amyloidosis. The sensitivity for detecting amyloid deposition was highest in biopsies of LSG at 89 %, followed by 77 % for bone marrow, and 72 % for skin. Amyloid deposition was detected in at least one superficial tissue of all the 18 patients. An LSG biopsy may be appropriate as a first-choice procedure to diagnose AL amyloidosis. Multiple biopsies of superficial tissues, including LSG, bone marrow, and skin, are recommended to increase the sensitivity for diagnosing AL amyloidosis.Entities:
Keywords: AL amyloidosis; Bone marrow; Labial salivary gland; Skin; Superficial tissue biopsy
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Year: 2015 PMID: 26555284 DOI: 10.1007/s00277-015-2549-y
Source DB: PubMed Journal: Ann Hematol ISSN: 0939-5555 Impact factor: 3.673