Chronic constipation and abdominal distension in a patient with adult Hirschprung’s disease and bilateral ovarian teratomas

Author:

Vo Jessica12,Hayler Raymond345,Tyler Alex6,Verschuer Kurt67

Affiliation:

1. Department of Obstetrics and Gynaecology, St George Hospital, Gray St George Hospital , Kogarah, Sydney, NSW , Australia

2. Faculty of Women’s Health, St George and Sutherland Clinical School (University of New South Wales), St George Hospital, Gray St, Kogarah , Sydney, NSW , Australia

3. Department of Surgery, St George Hospital , Gray St, Kogarah, Sydney, NSW , Australia

4. Faculty of Medicine & Health, St George and Sutherland Clinical School (University of New South Wales), St George Hospital, Gray St, Kogarah , Sydney, NSW , Australia

5. Faculty of Medicine and Health, Macquarie University , Technology Pl, Macquarie Park, Sydney, NSW , Australia

6. Department of Surgery, Shoalhaven District Memorial Hospital , Scenic Dr, Nowra, NSW , Australia

7. Department of Surgery, Goulburn Base Hospital , 130 Goldsmith St, Goulburn, NSW , Australia

Abstract

Abstract Hirschprung’s disease is a congenital disorder characterized by aganglionic bowel, usually diagnosed in infancy. Here, we present a unique case of Hirschprung’s disease diagnosed in a 29-year-old female with acute on chronic constipation. As part of her work up, a computerized tomography of her abdomen and pelvis revealed large, bilateral dermoid cysts. A diagnostic and therapeutic colonoscopy allowed manual disimpaction and decompression of her bowel, as well as biopsy attainment. Histopathology revealed absence of ganglionic cells on haematoxylin and eosin stain and calretinin immunostaining. This case underscores the diagnostic challenges of Adult Hirschprung’s disease and how this impacts patient quality of life, as well as the work up and management of concurrent causes abdominopelvic conditions.

Publisher

Oxford University Press (OUP)

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