| Literature DB >> 12114636 |
Kunihiko Seki, Shingo Wakatsuki, Kazuo Hizawa, Tadashi Hasegawa, Yuichi Fujinaka, Hiroshi Yokogoshi, Shiro Saito, Toshiaki Sano.
Abstract
Reports on patients with systemic amyloidosis-associated plasma cell dyscrasia (PCD) who have multiple endocrine tumors are very rare. Here we describe such a case. The patient was a 74-yr-old man with amyloid light-chain (AL) amyloidosis-associated PCD who had a null-cell adenoma of the pituitary and a latent papillary carcinoma of the thyroid gland. as well as a tubular adenoma of the sigmoid colon. The amyloid protein deposits reacted with the antibody to the n-immunoglobulin light chain. Since PCD by itself may be a risk factor for the development of subsequent neoplasms, the careful clinical evaluation of PCD patients is recommended.Entities:
Year: 1997 PMID: 12114636 DOI: 10.1007/BF02739944
Source DB: PubMed Journal: Endocr Pathol ISSN: 1046-3976 Impact factor: 4.056