Lynch syndrome is a genetic disease, caused by a germ-line mutation in a mismatch repair gene, related to an increased risk of developing colorectal and extracolonic cancer. Despite that, the incidence of primary peritoneal cancer after adnexectomy remains unknown. We here report a case of primary peritoneal cancer in a woman affected by Lynch syndrome who underwent hysterectomy+salpingo-oophorectomy for endometrial cancer 13 yr before. Morphology and immunophenotype allowed to differentiate peritoneal malignancy from the previously diagnosed endometrial carcinoma. Physicians should be aware of the potential risk of primary peritoneal cancer in women affected by Lynch syndrome, despite previous prophylactic surgery.

Lynch syndrome is a genetic disease, caused by a germ-line mutation in a mismatch repair gene, related to an increased risk of developing colorectal and extracolonic cancer. Despite that, the incidence of primary peritoneal cancer after adnexectomy remains unknown. We here report a case of primary peritoneal cancer in a woman affected by Lynch syndrome who underwent hysterectomy+salpingo-oophorectomy for endometrial cancer 13 yr before. Morphology and immunophenotype allowed to differentiate peritoneal malignancy from the previously diagnosed endometrial carcinoma. Physicians should be aware of the potential risk of primary peritoneal cancer in women affected by Lynch syndrome, despite previous prophylactic surgery.

Primary peritoneal cancer in Lynch syndrome: a clinical-pathologic report of a case and analysis of the literature / Ghezzi, F; Uccella, S; Cromi, A; Bogani, G; Donadello, N; Riva, C.. - In: INTERNATIONAL JOURNAL OF GYNECOLOGICAL PATHOLOGY. - ISSN 0277-1691. - 32:(2013), pp. 163-166. [10.1097/PGP.0b013e31825ac5c9]

Primary peritoneal cancer in Lynch syndrome: a clinical-pathologic report of a case and analysis of the literature.

Bogani G;
2013

Abstract

Lynch syndrome is a genetic disease, caused by a germ-line mutation in a mismatch repair gene, related to an increased risk of developing colorectal and extracolonic cancer. Despite that, the incidence of primary peritoneal cancer after adnexectomy remains unknown. We here report a case of primary peritoneal cancer in a woman affected by Lynch syndrome who underwent hysterectomy+salpingo-oophorectomy for endometrial cancer 13 yr before. Morphology and immunophenotype allowed to differentiate peritoneal malignancy from the previously diagnosed endometrial carcinoma. Physicians should be aware of the potential risk of primary peritoneal cancer in women affected by Lynch syndrome, despite previous prophylactic surgery.
2013
Lynch syndrome is a genetic disease, caused by a germ-line mutation in a mismatch repair gene, related to an increased risk of developing colorectal and extracolonic cancer. Despite that, the incidence of primary peritoneal cancer after adnexectomy remains unknown. We here report a case of primary peritoneal cancer in a woman affected by Lynch syndrome who underwent hysterectomy+salpingo-oophorectomy for endometrial cancer 13 yr before. Morphology and immunophenotype allowed to differentiate peritoneal malignancy from the previously diagnosed endometrial carcinoma. Physicians should be aware of the potential risk of primary peritoneal cancer in women affected by Lynch syndrome, despite previous prophylactic surgery.
Endometrial Neoplasms; complications/pathology/surgery; Female; Genetic Predisposition to Disease; Germ-Line Mutation; Humans; Hysterectomy; Middle Aged; MutS Homolog 2 Protein; genetics; Ovariectomy; Peritoneal Neoplasms; complications/drug therapy/pathology; Salpingectomy; ectal Neoplasms; Hereditary Nonpolyposis; complications/genetics
01 Pubblicazione su rivista::01a Articolo in rivista
Primary peritoneal cancer in Lynch syndrome: a clinical-pathologic report of a case and analysis of the literature / Ghezzi, F; Uccella, S; Cromi, A; Bogani, G; Donadello, N; Riva, C.. - In: INTERNATIONAL JOURNAL OF GYNECOLOGICAL PATHOLOGY. - ISSN 0277-1691. - 32:(2013), pp. 163-166. [10.1097/PGP.0b013e31825ac5c9]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1584299
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