scholarly journals Case Report: A Child With Functional Chronic Duodenal Obstruction Caused by Megaduodenum

2021 ◽  
Vol 8 ◽  
Author(s):  
Zhibo Qu ◽  
Biao Zheng ◽  
Chuncheng Ju ◽  
Jiaxu Liu ◽  
Bingyang Liu ◽  
...  
Keyword(s):  
Case Report ◽  
Duodenal Obstruction ◽  
Clinical Syndrome ◽  
Mechanical Obstruction ◽  
Congenital Disease ◽  
Paper Report

Megaduodenum is a clinical syndrome which is characterized by the remarkable expansion of duodenum. Megaduodenum can be caused by mechanical or functional chronic duodenal obstruction. Functional chronic duodenal obstruction of megaduodenum in children is a clinical syndrome characterized by non-mechanical obstruction of the duodenum and marked expansion. It is an extremely rare congenital disease. Our paper report a 1-year-old girl with functional chronic duodenal obstruction caused by megaduodenum.

Duodenal Obstruction and Acquired Gastroduodenal Fistula Caused by Magnets: A Case Report

2008 ◽  
Vol 58 (4) ◽  
pp. 405
Author(s):  
Il Joong Kim ◽  
Dong Hun Kim ◽  
Joo Nam Byun ◽  
Hyung Geun Lim
Keyword(s):  
Case Report ◽  
Duodenal Obstruction

OBTURATOR HERNIA: A CASE REPORT

2016 ◽  
pp. 106-109
Author(s):  
Hoang Minh Thi Nguyen ◽  
Huu Tri Nguyen ◽  
Thanh Thao Nguyen
Keyword(s):  
Computed Tomography ◽  
Case Report ◽  
Intestinal Obstruction ◽  
Key Words ◽  
Clinical Manifestation ◽  
Elderly Women ◽  
Obturator Hernia ◽  
Abdominal Hernia ◽  
Mechanical Obstruction

Obturator hernia is a rare pelvic hernia which accounts for 1% of all abdominal hernia. Clinical manifestation is ussually unspecific. Obturator hernia is often diagnosed by computed tomography or ultrasound. We present a case of obturator hernia in an elderly women who was successfully diagnosed and treated at Hue Univeristy of Medicine and Pharmacy. Key words: obturator hernia, mechanical obstruction, intestinal obstruction, Richter obturator hernia, strangulation

scholarly journals A UNUSAL PRESENTATION OF BARTTER SYNDROME

2019 ◽  
pp. 5-6
Author(s):  
Nitharsha Prakash M ◽  
N Nag Anand
Keyword(s):  
Case Report ◽  
Acute Gastroenteritis ◽  
Bartter Syndrome ◽  
Infants And Children ◽  
Renal Tubules ◽  
Adult Onset ◽  
Congenital Disease ◽  
Salt Wasting

Bartter Syndrome is a rare congenital disease that manifests as hypokalemia, hyponatremia and hypotension. The disease occurs due to defective genes that are responsible for the reabsorption of certain electrolytes in the renal tubules. Hence it results in salt-wasting dyselectrolytemia. By its inheritable nature, the usual presentation of the disease is in the infants and children. But this case report presents an adult with symptoms of Bartter Syndrome which was discovered by chance while the patient was being treated for Acute gastroenteritis. Adult onset of Bartter Syndrome is incredibly rare and has been reported only in few other cases.

scholarly journals ANNULAR PANCREAS CAUSING DUODENAL OBSTRUCTION: A CASE REPORT

2016 ◽  
Vol 5 (05) ◽  
pp. 296-300
Author(s):  
Swish Kumar Singh ◽  
Dinesh Kumar Agrawal ◽  
Suganita Suganita ◽  
Singh G N ◽  
Amar Kumar Singh
Keyword(s):  
Case Report ◽  
Duodenal Obstruction ◽  
Annular Pancreas

scholarly journals SINDROM TOLOSA HUNT DENGAN KETERLIBATAN SARAF OPTIKUS

2019 ◽  
Vol 37 (1) ◽  
Author(s):  
Astra Dea Simanungkalit ◽  
Maria Larasati Susyono ◽  
Vivien Puspitasari
Keyword(s):  
Visual Acuity ◽  
Case Report ◽  
Optic Nerve ◽  
Pain Relief ◽  
Clinical Syndrome ◽  
Orbital Apex ◽  
Corticosteroid Administration ◽  
Hunt Syndrome ◽  
Nerve Dysfunction ◽  
Optic Nerve Involvement

TOLOSA HUNT SYNDROME WITH OPTIC NERVE INVOLVEMENTABSTRACTTolosa Hunt syndrome (THS) is a very rare clinical syndrome, which is characterized by unilateral headaches accompanied by dysfunction and painful ophthalmic nerves. In some cases, optic nerve involvement can be found due to inflammation at the orbital apex. Corticosteroid administration is a management of THS with pain relief generally occurring in the first 72 hours. However, corticosteroid administration is not significantly associated with nerve dysfunction or visual acuity improvement.This article is a case report of women with STH and optic nerve involvement.Keywords: Tolosa Hunt syndrome, painful ophtalmoplegia, orbital apex, superior orbital fissureABSTRAKSindrom Tolosa Hunt (STH) adalah sindrom klinik yang sangat jarang, yang ditandai oleh nyeri kepala unilateral disertai disfungsi dan nyeri saraf penggerak bola mata (painful ophtamloplegia). Pada beberapa kasus, dapat ditemukan keterlibatan saraf optikus akibat inflamasi pada apeks orbita. Pemberian kortikosteroid merupakan tatalaksana STH dengan perbaikan nyeri umumnya terjadi pada 72 jam pertama. Meskipun demikian pemberian kortikosteroid tidak berhubungan secara signifikan dengan perbaikan disfungsi saraf penggerak bola mata maupun tajam penglihatan. Artikel ini merupakan laporan kasus perempuan dengan STH dan keterlibatan saraf optikus.Kata kunci: Sindrom Tolosa Hunt, painful ophtalmoplegia, apeksorbita, fisura orbitalis superior

scholarly journals Complete duodenal obstruction induced by groove pancreatitis: A case report

2019 ◽  
Vol 7 (23) ◽  
pp. 4106-4110 ◽  
Author(s):  
Ya-Li Wang ◽  
Chen-Hao Tong ◽  
Jian-Hua Yu ◽  
Zhi-Liang Chen ◽  
Hong Fu ◽  
...  
Keyword(s):  
Case Report ◽  
Duodenal Obstruction ◽  
Groove Pancreatitis

Large Uterine Fibroids Causing Mechanical Obstruction of the Inferior Vena Cava and Subsequent Thrombosis: A Case Report

2006 ◽  
Vol 40 (5) ◽  
pp. 425-427 ◽  
Author(s):  
Jenny Hawes ◽  
Joann Lohr ◽  
Barry Blum ◽  
Anant Bhati ◽  
Jayapandia Bhaskaran ◽  
...  
Keyword(s):  
Case Report ◽  
Inferior Vena Cava ◽  
Inferior Vena ◽  
Vena Cava ◽  
Uterine Fibroids ◽  
Mechanical Obstruction

scholarly journals Incidental Finding of Annular Pancreas in a Routine Cadaveric Dissection: Case Report

2019 ◽  
Vol 36 (04) ◽  
pp. 299-302
Author(s):  
Mythraeyee Prasad ◽  
Theresa Susan Kuriakose ◽  
Sipra Rout
Keyword(s):  
Congenital Anomaly ◽  
Case Report ◽  
Duodenal Obstruction ◽  
Clinical Symptoms ◽  
Incidental Finding ◽  
Age Groups ◽  
Annular Pancreas ◽  
Present Case Report ◽  
Rare Congenital Anomaly ◽  
Variable Presentation

AbstractAnnular pancreas is a rare congenital anomaly that results from the malrotation of the ventral pancreatic bud. The presentation of annular pancreas varies: it can be asymptomatic or present clinical symptoms of duodenal obstruction that can affect all age groups, from newborns to adults. In the present case report, we describe a complete type of annular pancreas at the level of the second part of the duodenum, which was an incidental finding in a prosected specimen. This anomaly has significant clinical relevance to clinicians and radiologists due to its variable presentation. The embryological, clinical and radiological aspects of this congenital anomaly are discussed in detail in the present article.

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