Results 61 to 70 of about 477,435 (129)

Total colonic tubular duplication causing severe constipation

Journal of Pediatric Surgery Case Reports, 2019
Aim: To report the case of a patient with total colonic tubular duplication pointing out the diagnostic and therapeutic difficulties and reviewing the Literature concerning this rare malformation.
Francesca Destro, Enrico La Pergola, Luciano Maestri, Milena Meroni, Claudio Vella, Giovanna Riccipetitoni   +5 more
doaj   +1 more source

Conservative Management Enabling Spontaneous Passage of an Idiopathic Primary Spontaneous Enterolith: A Case Report and Literature Review

Clinical Case Reports, Volume 14, Issue 7, July 2026.
ABSTRACT Enterolithiasis—formation of stone concretions within the gastrointestinal tract—is an uncommon and underrecognized cause of intermittent abdominal symptoms and acute bowel obstruction. Primary (true) enteroliths originate within the bowel lumen and are usually associated with focal stasis from anatomic or inflammatory pathology; idiopathic ...
Lensa Million Baharu, Ragasa Getachew Bayisa, Zenebe Teklu Gebremariam, Esmael Mohamed Dawud, Nigusu Solomon Herego, Nahom Teklu Maru, Webi Alemayehu Tulu, Ahmedin Solomon Kedir, Tamirat Godebo Woyimo   +8 more
wiley   +1 more source

Females with externally visible but stenosed fecal orifice – low or high anorectal malformation

Journal of Indian Association of Pediatric Surgeons, 2017
We report four female children with externally visible but stenosed fecal orifice which proved to be a high anorectal malformation (Type IV pouch colon). They were managed by an abdominoperineal approach with excellent results.
Pavai Arunachalam, Sudipta Sen, Cenita J Sam, B Meenalosani   +3 more
doaj   +1 more source

Rare association of prune belly syndrome with pouch colon

, 2011
M Ragavan1, U Haripriya1, PV Pradeep1, J Sarvavinothini21Department of Endocrine Surgery, 2Department of Anaesthesia, Narayana Medical College and Superspeciality Hospital, Nellore, Andhra Pradesh, IndiaAbstract: Prune belly syndrome is a triad ...
U Haripriya, PV Pradeep, et al, M Ragavan   +3 more
core  

A Cross‐Organ Symphony of Human Immune System Maturation

Organ Medicine, Volume 3, Issue 3, Page 125-127, September 2026.
Zhan‐Li Chen
wiley   +1 more source

A female patient with congenital pouch colon (cpc): A case report

, 2011
Congenital short colon, more commonly known as pouch colon, is a rare anomaly that can be encountered with anorectal malformations (ARM). The colon is shorter than normal and the distal end is dilated like a pouch.
Ayhan S., Yilmaz O., Aygoren R., Genc A., Taneli C., Ozcan T.   +5 more
core   +1 more source

Type V Pouch Colon, Prune Belly Syndrome, and Congenital Anterior Urethrocutaneous Fistula

, 2017
Congenital pouch colon (CPC) or short colon syndrome is a rare type of anorectal malformation(ARM). Type V is the rarest form of CPC. We present a 1-day-old male child with type V CPC with prune belly syndrome and congenital anterior urethrocutaneous ...
Prince Raj, Hirendra Birua
core   +1 more source

Two-staged management for all types of congenital pouch colon

, 2014
Background: The aim of this study was to review our experience with two-staged management for all types of congenital pouch colon (CPC).Patients and Methods: This retrospective study included CPC cases that were managed with two-staged procedures in the ...
Budhwani, KS, Ghritlaharey, RK
core   +1 more source

Congenital Pouch Colon in a Neonate. [PDF]

Pak J Med Sci, 2022
Niaz S, Naz S, Raziq RA.
europepmc   +1 more source

Congenital pouch colon: Case report and literature review. [PDF]

Ann Med Surg (Lond), 2022
Qafisheh Q, Zaolloum J, Hussein A, Yahya RM, Abuzneid YS, Ghazzawi I, Karsh RA.   +6 more
europepmc   +1 more source