scholarly journals Abdominal Cocoon in an Adolescent Male

2014 ◽  
Vol 10 (4) ◽  
pp. 83-86 ◽  
Author(s):  
VC Shakya ◽  
CS Agrawal ◽  
SK Rajbanshi ◽  
A Pradhan ◽  
S Khaniya ◽  
...  

Abdominal cocoon is an uncommon peritoneal condition characterized by partial or complete encasement of small bowel by a thick rind of fibrous tissue and adhesions. Only few cases of this disease have been reported in world literature. The etiology of this condition is unknown, and most often it is found in adolescent girls from tropical or subtropical countries, and usually diagnosed incidentally on exploration. Surgery (membrane dissection and extensive adhesiolysis) is the treatment of choice. Here, we report a case of abdominal cocoon in a 20-year-old male patient, with a brief review of the literature. DOI: http://dx.doi.org/10.3126/kumj.v10i4.11009 Kathmandu Univ Med J 2012;10(4):83-86

2009 ◽  
Vol 39 (4) ◽  
pp. 254-256 ◽  
Author(s):  
N A Ibrahim ◽  
M A Oludara

2011 ◽  
Vol 93 (6) ◽  
pp. e81-e82 ◽  
Author(s):  
MAS Khan ◽  
R Price ◽  
EP Dewar

Intussusception through loop ileostomy is rare and must be treated without delay to avoid further complications. Retrograde intussusception is even rarer. We report a case of small bowel obstruction caused by retrograde intussusception through the distal limb of loop ileostomy in a male patient. A literature search is also carried out regarding this entity and published reports are discussed.


2011 ◽  
Vol 2011 ◽  
pp. 1-5 ◽  
Author(s):  
Ibrahim E. Bassiouny ◽  
Tariq O. Abbas

We have treated two patients with small bowel (abdominal) cocoon who presented with acute and partial small bowel obstruction associated with an abdominal mass. Neither had a history of previous surgery, peritonitis, or prolonged drug therapy. The distinct features of this disease are illustrated. A developmental etiology and a new nomenclature for this disease are proposed, along with a review of the literature.


2019 ◽  
Vol 2019 (12) ◽  
Author(s):  
Catharine Kappauf ◽  
Jamal Rahaman ◽  
Daniel Popowich

Abstract Abdominal cocoon is the idiopathic fibrotic encasement of abdominal organs. It classically presents as small bowel obstruction in young women. In this case report, we present a rare example of a patient presenting solely with massive ascites of presumed gynecologic origin, who upon surgical exploration was found to have abdominal cocoon. We discuss the patient’s unique disease presentation, unrevealing work-up and the treatment strategy pursued, and provide a review of the literature.


2014 ◽  
Vol 86 (9) ◽  
Author(s):  
Mariusz Wesecki ◽  
DaGmara Radziuk ◽  
Szymon Niemiec ◽  
Dariusz Waniczek ◽  
Zbigniew Lorenc

AbstractCalcifying fibrous tumor is a rare disease entity, usually concerning the soft tissues of the limbs, neck, trunk, or scrotum. Cases of the above-mentioned pathology have also been reported considering the pleural and peritoneal cavity, and small bowel mesentery. The essence of the disease, whose etiology and pathogenesis remains unclear, is the fibrous tissue infiltration and diffuse inflammation with focal calcifications. The study presented a case of a 27-year old male patient subjected to surgical intervention, due to an abdominal cavity tumor. The tumor was radically removed, and its character and definitive diagnosis were established postoperatively. After a seven-year follow-up period, recurrence was not observed.


Author(s):  
Aleksandra Gilis-Januszewska ◽  
Malgorzata Wilusz ◽  
Renata Turek-Jabrocka ◽  
Jacek Pantoflinski ◽  
Malgorzata Trofimiuk-Muldner ◽  
...  

2019 ◽  
Vol 3 (4) ◽  
pp. 275-278
Author(s):  
Jonathan Bellew ◽  
Chad Taylor ◽  
Jaldeep Daulat ◽  
Vernon Mackey

Pyogenic granulomas are vascular hyperplasias presenting as red papules, polyps, or nodules on the gingiva, fingers, lips, face and tongue of children and young adults.  Most commonly they are associated with trauma, but systemic retinoids have rarely been implicated as a causative factor in their appearance.  We present a case of spontaneous eruption of multiple pyogenic granulomas of the bilateral periungal fingers in an otherwise healthy adolescent male undergoing isotretinoin therapy for severe nodulocystic acne. These pyogenic granulomas did not resolve spontaneously with discontinuation of isotretinoin, or first line therapeutic modalities. Their resolution did occur with administration of intralesional steroids and ablation with silver nitrate.


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