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Morphologic characterization of hamartomatous gastrointestinal polyps in Cowden syndrome, Peutz-Jeghers syndrome, and juvenile polyposis syndrome.
Shaco-Levy, Ruthy; Jasperson, Kory W; Martin, Katie; Samadder, N Jewel; Burt, Randall W; Ying, Jian; Bronner, Mary P.
Afiliación
  • Shaco-Levy R; Department of Pathology, Soroka Medical Center, Ben-Gurion University of the Negev, Beer Sheva 84101, Israel; Department of Pathology & ARUP Laboratories, University of Utah, Salt Lake City, UT 84112; Huntsman Cancer Institute, University of Utah, Salt Lake City, UT 84112. Electronic address: rs
  • Jasperson KW; Huntsman Cancer Institute, University of Utah, Salt Lake City, UT 84112; Genetic Counseling, University of Utah, Salt Lake City, UT 84112.
  • Martin K; Genetic Counseling, University of Utah, Salt Lake City, UT 84112.
  • Samadder NJ; Huntsman Cancer Institute, University of Utah, Salt Lake City, UT 84112; Department of Internal Medicine, University of Utah, Salt Lake City, UT 84112; Division of Gastroenterology, University of Utah, Salt Lake City, UT 84112.
  • Burt RW; Huntsman Cancer Institute, University of Utah, Salt Lake City, UT 84112; Department of Internal Medicine, University of Utah, Salt Lake City, UT 84112; Division of Gastroenterology, University of Utah, Salt Lake City, UT 84112.
  • Ying J; Huntsman Cancer Institute, University of Utah, Salt Lake City, UT 84112; Department of Internal Medicine, University of Utah, Salt Lake City, UT 84112; Division of Epidemiology, University of Utah, Salt Lake City, UT 84112.
  • Bronner MP; Department of Pathology & ARUP Laboratories, University of Utah, Salt Lake City, UT 84112; Huntsman Cancer Institute, University of Utah, Salt Lake City, UT 84112.
Hum Pathol ; 49: 39-48, 2016 Mar.
Article en En | MEDLINE | ID: mdl-26826408
The morphologic features of the gastrointestinal polyps in hamartomatous polyposis syndromes are poorly defined. Our aim was to better characterize the gastrointestinal hamartomas in these syndromes. A blinded review was performed regarding many histologic features for every polyp. The study included 15 Cowden syndrome, 13 Peutz-Jeghers (PJS), 12 juvenile polyposis (JuvPS) patients, and 32 cases of sporadic hamartomatous polyps. A total of 375 polyps were examined. Cowden syndrome polyps were characteristically colonic, sessile, small, without surface erosion, and showing mildly inflamed fibrotic lamina propria with smooth muscle proliferation and lymphoid follicles. They showed the least degree of cystic glands and had no thick mucin. Uncommon but specific features were ganglion cells and nerve fibers within the lamina propria and mucosal fat. PJS polyps were typically of small or large bowel origin, often exophytic, seldom eroded, with inflamed edematous and fibrotic lamina propria and dilated cystic glands filled with often thick mucin. All PJS polyps showed smooth muscle proliferation, frequently widespread. The polyps of JuvPS were typically colonic, large, exophytic, eroded, with strikingly edematous, fibrotic markedly inflamed lamina propria, cystic glands filled with frequently thick mucin, and the least degree of smooth muscle proliferation. Nonsyndromic hamartomatous polyps were similar to JuvPS polyps; however, they were more often colonic, were smaller, showed more widespread smooth muscle proliferation, and were less likely to contain thick mucin. In conclusion, we were able to define the characteristic hamartomatous polyp for each hamartomatous polyposis syndrome. Awareness to these features may aid in the diagnosis of these rare syndromes.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de Hamartoma Múltiple / Síndromes Neoplásicos Hereditarios / Síndrome de Peutz-Jeghers / Pólipos del Colon / Poliposis Intestinal Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans País/Región como asunto: America do norte Idioma: En Revista: Hum Pathol Asunto de la revista: PATOLOGIA Año: 2016 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de Hamartoma Múltiple / Síndromes Neoplásicos Hereditarios / Síndrome de Peutz-Jeghers / Pólipos del Colon / Poliposis Intestinal Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans País/Región como asunto: America do norte Idioma: En Revista: Hum Pathol Asunto de la revista: PATOLOGIA Año: 2016 Tipo del documento: Article Pais de publicación: Estados Unidos