Literature DB >> 1421720

Thyroid papillary adenocarcinoma in a woman with Peutz-Jeghers syndrome.

M Yamamoto1, H Hoshino, T Onizuka, M Ichikawa, A Kawakubo, S Hayakawa.   

Abstract

We present a rare case of Peutz-Jeghers(P-J) syndrome in a 29-year-old woman who developed adenocarcinoma of the thyroid and polyps in the gastrointestinal tract. Polyps removed from the stomach, colon and ileum showed features typical of hamartomas. Histological examination indicated that the tumor resected from the right lobe of the thyroid was a papillary adenocarcinoma. This appears to be the first precise report of a P-J syndrome associated with thyroid carcinoma. This case adds an example of predisposition of P-J syndrome to extra-intestinal malignancy and indicates the importance of long-term observation of malignancy.

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Year:  1992        PMID: 1421720     DOI: 10.2169/internalmedicine.31.1117

Source DB:  PubMed          Journal:  Intern Med        ISSN: 0918-2918            Impact factor:   1.271


  3 in total

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3.  STK11 Mutation Identified in Thyroid Carcinoma.

Authors:  Shuanzeng Wei; Virginia A LiVolsi; Marcia S Brose; Kathleen T Montone; Jennifer J D Morrissette; Zubair W Baloch
Journal:  Endocr Pathol       Date:  2016-03       Impact factor: 3.943

  3 in total

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