Peutz-jeghers syndrome associated with adenocarcinoma of the cecum and focal carcinomas in hamartomatous polyps of the colon: A case report

1991 ◽  
Vol 21 (2) ◽  
pp. 220-223 ◽  
Author(s):  
Ken Niimi ◽  
Hirotsugu Tomoda ◽  
Motonosuke Furusawa ◽  
Itsurou Hayashi ◽  
Yukiya Okumura
Keyword(s):  
Case Report ◽  
Hamartomatous Polyps ◽  
Peutz Jeghers Syndrome

Biliary cirrhosis secondary to bile duct obstruction by hamartomatous polyps in a patient with Peutz–Jeghers syndrome. Case Report

2017 ◽  
Vol 40 (7) ◽  
pp. 459-462
Author(s):  
Miguel Angel Vichido-Luna ◽  
Flora Zárate-Mondragón ◽  
María Antonieta Mora-Tiscareño ◽  
Roberto Cervantes-Bustamante ◽  
Jaime Alfonso Ramírez-Mayans
Keyword(s):  
Case Report ◽  
Bile Duct ◽  
Bile Duct Obstruction ◽  
Biliary Cirrhosis ◽  
Hamartomatous Polyps ◽  
Duct Obstruction ◽  
Peutz Jeghers Syndrome

scholarly journals PeutzJeghers syndrome: A case report and literature review

2014 ◽  
Vol 4 (8) ◽  
pp. 677-679
Author(s):  
A Lakhey ◽  
H Shakya
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Physical Examination ◽  
Rectal Bleeding ◽  
Buccal Mucosa ◽  
Autosomal Dominant ◽  
Hamartomatous Polyps ◽  
Pigmented Lesions ◽  
History Of ◽  
Peutz Jeghers Syndrome

Peutz–Jeghers Syndrome is an autosomal dominant inheritedhamartomatous polyp. We present a case of a 5-year-old young boywith a history of per rectal bleeding and mass protruding out of the anus. Physical examination revealed presence of mucocutaneous pigmented lesions over the tongue, and few hamartomatous polyps protruding out of the rectum suggesting Peutz–Jeghers syndrome. The presence in early infancy of small, well-demarcated and dark-brown to blue-black lentigines on the lips,buccal mucosa and perioral skin, should alert the clinician to Peutz–Jeghers Syndrome.DOI: http://dx.doi.org/10.3126/jpn.v4i8.11597 Journal of Pathology of Nepal; Vol.4,No. 8 (2014) 677-679

scholarly journals Unexpected Peutz-Jeghers Syndrome in an Adult Presenting with Intermittent Upper Intestinal Obstruction. A Case Report

2014 ◽  
Vol 23 (1) ◽  
pp. 91-94
Author(s):  
Paula Szanto ◽  
Valentina Barbieru ◽  
Radu Badea ◽  
Teodora Pop ◽  
Ioana Rusu ◽  
...  
Keyword(s):  
Case Report ◽  
Gastrointestinal Tract ◽  
Intestinal Obstruction ◽  
Autosomal Dominant ◽  
Inherited Disease ◽  
Hamartomatous Polyps ◽  
Atypical Form ◽  
Hamartomatous Polyposis Syndromes ◽  
Polyposis Syndromes ◽  
Peutz Jeghers Syndrome

Peutz-Jeghers syndrome is an autosomal dominant inherited disease, belonging to the hamartomatous polyposis syndromes. It is characterized by multiple hamartomatous polyps of the gastrointestinal tract associated with oral and anal mucocutaneous pigmentations. We report the case of an adult patient diagnosed with an atypical form of Peutz-Jeghers syndrome, thereby emphasizing the different possible syndrome phenotypes and the difficulty of their diagnosis.

scholarly journals Bladder hamartoma in Peutz-Jeghers syndrome: a rare case report

2021 ◽  
Vol 27 (1) ◽  
Author(s):  
Jai Kumar ◽  
Mohammad Irfaan Albeerdy ◽  
Nadeem Ahmed Shaikh ◽  
Abdul Hafeez Qureshi
Keyword(s):  
Urinary Bladder ◽  
Filling Defect ◽  
Hamartomatous Polyps ◽  
Case Presentation ◽  
Rare Case Report ◽  
Mucocutaneous Pigmentation ◽  
Dominant Disease ◽  
Peutz Jeghers Syndrome ◽  
Comprehensive Compilation

Abstract Background Peutz-Jeghers syndrome is an autosomal dominant disease characterized by mucocutaneous pigmentation and hamartomatous polyps in the gastrointestinal tract (GIT). There have also been cases of extra GIT polyps such as the renal pelvis, urinary bladder, lungs and nares. Bladder hamartoma is an extremely rare finding, with only 12 cases described in the literature up to now. The rarity of the condition necessitates a comprehensive compilation of managements up to now so as to provide a better tool for the treatment of such conditions in the future. Case presentation A twenty-year-old male, known to have Peutz-Jeghers syndrome, presented to us complaining of obstructive urinary symptoms. A urethrogram done showed a filling defect at the base of the urinary bladder. The mass was resected transurethrally, and histopathology revealed a hamartoma of the bladder. The patient has since remained tumor-free on follow-up. Conclusions Transurethral resection of the bladder mass proved to be an effective therapy in this patient with no recurrence on the patient’s follow-up till now. There is still, however, a dearth of knowledge regarding the management of bladder hamartomas owing to the extreme rarity of the case.

scholarly journals Peutz-Jeghers syndrome in a woman presenting as intussusception: A case report

2021 ◽  
Vol 79 ◽  
pp. 286-290
Author(s):  
Erwin Syarifuddin ◽  
Rina Masadah ◽  
Ronald Erasio Lusikooy ◽  
Warsinggih ◽  
Julianus Aboyaman Uwuratuw ◽  
...  
Keyword(s):  
Case Report ◽  
Peutz Jeghers Syndrome

scholarly journals Hamartomatous Polyps and Associated Syndromes

2016 ◽  
Vol 29 (04) ◽  
pp. 330-335 ◽  
Author(s):  
Molly Cone
Keyword(s):  
Colorectal Cancer ◽  
Gastrointestinal Tract ◽  
Autosomal Dominant ◽  
Juvenile Polyposis Syndrome ◽  
Inherited Disorders ◽  
Polyposis Syndrome ◽  
Hamartomatous Polyps ◽  
Hereditary Syndromes ◽  
Colon And Rectum ◽  
Peutz Jeghers Syndrome

AbstractHamartomatous polyps of the gastrointestinal tract can occur sporadically, however, for several hereditary syndromes, their presence is one of the major clinical features. Peutz–Jeghers syndrome, juvenile polyposis syndrome, and the PTEN hamartoma syndromes are autosomal dominant inherited disorders that predispose to formation of such polyps, especially in the colon and rectum. These can lead to increased colorectal cancer risk and should be followed and managed appropriately. In this article, the three major hereditary hamartomatous syndromes are described, including presentation, colorectal surveillance, and management.

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