Peritoneal pseudomyxoma in a child with a gallbladder Peutz-Jeghers-Like hamartomatous polyp: A case report

1998 ◽  
Vol 33 (8) ◽  
pp. 1320-1322 ◽  
Author(s):  
Pablo Guzmán ◽  
Iván Roa ◽  
Miguel Villaseca ◽  
Juan Carlos Roa ◽  
Juan Carlos Araya
2015 ◽  
Vol 9 (1) ◽  
Author(s):  
Michael Pitiakoudis ◽  
Konstantinos Romanidis ◽  
Alexandra Giatromanolaki ◽  
Nikos Courcoutsakis ◽  
Eleni-Aikaterini Nagorni ◽  
...  

2017 ◽  
Vol 20 (6) ◽  
pp. 774 ◽  
Author(s):  
DK Mundi ◽  
M Singh ◽  
I Kaur ◽  
A Kaur

2017 ◽  
Vol 71 (S3) ◽  
pp. 1727-1729 ◽  
Author(s):  
Amitav Shukla ◽  
Trishna Kakad ◽  
Saloni Shah ◽  
Anita S. Bhaduri

2021 ◽  
Vol 8 (10) ◽  
pp. 3168
Author(s):  
Gajendra Anuragi ◽  
Afroz I. Bagwan ◽  
Ramprakash V. S. ◽  
Sugumar C. ◽  
Naganath B. O. Lakshmanamoorthy

Peutz Jeghers syndrome is an autosomal dominant hereditary disorder affecting male and female equally. It is characterised by mucocutaneous hyperpigmentation and hamartomatous polyp in gastrointestinal tract with increased risk of malignancy. We report here a case of 52-year-old patient with traits of Peutz jeghers syndrome presented with acute intestinal obstruction following colocolic intussusception. Peutz jeghers syndrome is an autosomal dominant inherited disorder. Individual may present in rare case with acute intestinal obstruction associated with intussusception due to polyps.


2017 ◽  
Vol 4 (2) ◽  
pp. C37-C39
Author(s):  
Kamal Nain Rattan ◽  
Shruti Bansal ◽  
Roomi Yadav ◽  
Gurupriya J ◽  
Neha Singh

2009 ◽  
Vol 42 (9) ◽  
pp. 1523-1527
Author(s):  
Takashi Nonaka ◽  
Hidetoshi Fukuoka ◽  
Hiroaki Takeshita ◽  
Terumitsu Sawai ◽  
Tomayoshi Hayashi ◽  
...  

1988 ◽  
Vol 18 (4) ◽  
pp. 475-477 ◽  
Author(s):  
Hideaki Naitoh ◽  
Yoshiaki Sumiyoshi ◽  
Ryunosuke Kumashiro ◽  
Sadamitsu Inutsuka ◽  
Kouichi Fujita ◽  
...  

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