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[Hamartomatous polyposis syndrome].
Nihon Rinsho. 1995 Nov; 53(11):2728-33.NR

Abstract

The hamartomatous polyposis syndromes, which comprise Peutz-Jeghers syndrome, juvenile polyposis, and Cowden's disease, occur less frequently. These disorders are characterized by multiple hamartomatous polyps in the gastrointestinal tract, and distinctive extraintestinal manifestations. We have recognized that these have inheritance with autosomal dominant trait by genetic studies. Most of them have high malignant potential which make transformation to neoplasms in gastrointestinal tract and extraintestinal organs. It is necessary for patients with these disorders to manage appropriately. Therefore, we must understand their natural histories and pathological characterization. Because affected patients and their first degree relatives belong to high risk groups of malignant neoplasms, we have to intensively survey them through their lifetime.

Authors+Show Affiliations

Department of Genetics, Hyogo College of Medicine.No affiliation info available

Pub Type(s)

English Abstract
Journal Article
Review

Language

jpn

PubMed ID

8538034

Citation

Tamura, K, and J Utsunomiya. "[Hamartomatous Polyposis Syndrome]." Nihon Rinsho. Japanese Journal of Clinical Medicine, vol. 53, no. 11, 1995, pp. 2728-33.
Tamura K, Utsunomiya J. [Hamartomatous polyposis syndrome]. Nippon Rinsho. 1995;53(11):2728-33.
Tamura, K., & Utsunomiya, J. (1995). [Hamartomatous polyposis syndrome]. Nihon Rinsho. Japanese Journal of Clinical Medicine, 53(11), 2728-33.
Tamura K, Utsunomiya J. [Hamartomatous Polyposis Syndrome]. Nippon Rinsho. 1995;53(11):2728-33. PubMed PMID: 8538034.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - [Hamartomatous polyposis syndrome]. AU - Tamura,K, AU - Utsunomiya,J, PY - 1995/11/1/pubmed PY - 1995/11/1/medline PY - 1995/11/1/entrez SP - 2728 EP - 33 JF - Nihon rinsho. Japanese journal of clinical medicine JO - Nippon Rinsho VL - 53 IS - 11 N2 - The hamartomatous polyposis syndromes, which comprise Peutz-Jeghers syndrome, juvenile polyposis, and Cowden's disease, occur less frequently. These disorders are characterized by multiple hamartomatous polyps in the gastrointestinal tract, and distinctive extraintestinal manifestations. We have recognized that these have inheritance with autosomal dominant trait by genetic studies. Most of them have high malignant potential which make transformation to neoplasms in gastrointestinal tract and extraintestinal organs. It is necessary for patients with these disorders to manage appropriately. Therefore, we must understand their natural histories and pathological characterization. Because affected patients and their first degree relatives belong to high risk groups of malignant neoplasms, we have to intensively survey them through their lifetime. SN - 0047-1852 UR - https://www.unboundmedicine.com/medline/citation/8538034/[Hamartomatous_polyposis_syndrome]_ DB - PRIME DP - Unbound Medicine ER -
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