Results 61 to 70 of about 5,824 (184)

Educational Case: Hirschsprung Disease

Academic Pathology, 2019
The following fictional case is intended as a learning tool within the Pathology Competencies for Medical Education (PCME), a set of national standards for teaching pathology.
Lauren Kroll-Wheeler MD, Allecia M. Wilson MD   +1 more
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Conditions that mimic Hirschsprung’s disease, but that are not Hirschsprung’s disease

World Journal of Pediatric Surgery
Hirschsprung’s disease (HSCR) is widely recognized in pediatric surgery. This condition has been elucidated, and therapeutic approaches have been developed. However, even when ganglion cells are present in the rectum, some patients still experience symptoms such as bowel obstruction, intestinal dilatation, and chronic constipation, which are similar to
Shun Onishi, Satoshi Ieiri
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Hirschsprung’s disease in adults

Acta chirurgica Iugoslavica, 2006
Hirschsprung?s disease is the malformation of the hindgut characterized by the absence of intramural ganglion cells in the submucosal and myenteric plexuses and manifested by megacolon. Congenital character of this disease stipulates its belonging in general to the scope of activity of the pediatric clinics.
G I, Vorobyov, S I, Achkasov, O M, Biryukov   +2 more
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SYMPTOMS AND DIAGNOSIS OF HIRSCHSPRUNG’S DISEASE

e-Jurnal Medika Udayana, 2014
Hirschsprung disease is a disease that attacks the human digestive system, mainly in the largeintestine (colon). In this disease, found enlargement of the colon (megacolon), due to the absenceof ganglion cells in the distal intestine.
Putu Ayu Ines Lassiyani Surya, I Made Dharmajaya   +1 more
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Hirschsprung-associated enterocolitis: a comprehensive review

World Journal of Pediatric Surgery
Hirschsprung-associated enterocolitis (HAEC) is an important cause of morbidity and the leading cause of mortality in patients with Hirschsprung disease.
Ioannis A Ziogas, Ming Fu, Korah P Kuruvilla, Ankush Gosain   +3 more
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Hirschsprung disease [PDF]

ANZ Journal of Surgery, 2017
King, SK, Karpelowsky, J
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Colorectal cancer at the anastomotic site following childhood surgery for hirschsprung disease: a rare case report

World Journal of Surgical Oncology
Background The present case of a colorectal adenocarcinoma at the anastomotic site of a colorectal anastomosis after childhood surgery for Hirschsprung disease is a rare report of such pathology.
Matthias Mehdorn, Philipp Rhode, Jan-Hendrik Gosemann, Katja Grunwald, Hans-Jonas Meyer, Martin Lacher, Sigmar Stelzner   +6 more
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Management of comorbid congenital diaphragmatic hernia and Hirschsprung disease: A case report

Journal of Pediatric Surgery Case Reports
Introduction: Congenital diaphragmatic hernia (CDH) and Hirschsprung disease (HD) are each rare, potentially life-threatening congenital diseases. Early recognition of combined presentation allows for optimal management.
Nzuekoh N. Nchinda, Carrie Foster, Jimiane Ashe, Matthew B. Dellinger, Samuel E. Rice-Townsend   +4 more
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TREATMENT OF HIRSCHSPRUNG DISEASE IN ADULTS

Acta Biomedica Scientifica, 2012
The article presents our own experience of treatment of Hirschsprung disease in adults.
I. S. Moskvitin, B. V. Zaigraev, A. N. Plekhanov, A. I. Tovarshinov   +3 more
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Síndrome de Currarino y enfermedad de Hirschsprung: Una asociación poco frecuente Currarino´s syndrome and Hirschsprung´s disease: A rare combination

Revista Chilena de Radiología, 2012
El Síndrome de Currarino consiste en agenesia sacra parcial de herencia genética autosómica dominante parcial, que afecta las vértebras sacras S2 a S5, preservándose S1.
David Ibáñez M, Ana Vela M, Beatriz Izquierdo H, Carolina Muel G   +3 more
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