scholarly journals Diphallia, a rare congenital anomaly- A case and literature review

2021 ◽  
Vol 7 (2) ◽  
pp. 51-53
Author(s):  
L Muhindo ◽  
◽  
AA Hadonou ◽  
IK Gandaho ◽  
Toré Sanni R ◽  
...  
Keyword(s):  
Congenital Anomaly ◽  
Literature Review ◽  
General Surgery ◽  
Rare Case ◽  
Urogenital System ◽  
Partial Duplication ◽  
Rare Congenital Anomaly ◽  
Centre Hospitalier ◽  
Centre Hospitalier Universitaire ◽  
Surgery Department

Diphallia or also called diphallus is a malformation of the male urogenital system characterized by a complete or partial duplication of the penis. The authors report one rare case of a newborn baby transferred from pediatrics for better management of a polymalformative syndrome associating diphallia and anal imperforation are treating in Urology unit at general surgery department, Centre hospitalier universitaire departemental Borgou-Alibori, at Parakou City

scholarly journals Congenital Agenesis of the Left Lung: A Rare Case

2011 ◽  
Vol 1 ◽  
pp. 47 ◽  
Author(s):  
Tülin Durgun Yetim ◽  
Hanifi Bayaroğullari ◽  
Hülya Polat Yalçin ◽  
Vefik Arιca ◽  
Seçil Gunher Arιca
Keyword(s):  
Congenital Anomaly ◽  
Rare Case ◽  
Left Lung ◽  
Urogenital System ◽  
Pulmonary Agenesis ◽  
Rare Congenital Anomaly ◽  
Congenital Agenesis

Pulmonary agenesis is a rare congenital anomaly, the etiology of which is not clearly known. Other systemic comorbidities such as cardiovascular, gastrointestinal, musculoskeletal, and urogenital system anomalies can be observed in more than half of the patients. It is usually diagnosed during childhood. Diagnosis in adulthood is very rare. We present a case of pulmonary agenesis diagnosed in an adult.

scholarly journals Caecal duplication cyst: rare case report with review of literature

2019 ◽  
Vol 6 (11) ◽  
pp. 4190
Author(s):  
Muthukumaran J. ◽  
Udhayasankar V.
Keyword(s):  
Congenital Anomaly ◽  
Rare Case ◽  
Alimentary Tract ◽  
Female Child ◽  
Duplication Cyst ◽  
Paediatric Surgery ◽  
Review Of Literature ◽  
Rare Congenital Anomaly ◽  
Rare Case Report ◽  
Surgery Department

Duplication cysts of the alimentary tract are very rare congenital anomaly. Out of all these cases, two-thirds of them manifest before the age of 2 years. They are common in ileum, but very rare in cecum. We hereby report a case of 6 years female child presented in paediatric surgery department with abdominal pain, diagnosed as duplication cyst with intussusceptions.

scholarly journals CASE REPORT : RARE CASE OF SMALL BOWEL OBSTRUCTION DUE TO MECKELS DIVERTICULUM

2021 ◽  
Vol 9 (06) ◽  
pp. 641-644
Author(s):  
Simranjit Kaur Dhadiala ◽  
◽  
Abhijit A. Whatkar ◽  
Keyword(s):  
Congenital Anomaly ◽  
Case Report ◽  
Gastrointestinal Tract ◽  
Small Bowel ◽  
Small Bowel Obstruction ◽  
Bowel Obstruction ◽  
Rare Case ◽  
Rare Congenital Anomaly ◽  
Meckels Diverticulum ◽  
Male To Female

Meckels diverticulum is a rare congenital anomaly of gastrointestinal tract, seen in 2% of population. It was first described by Guilhemus Fabricus Hildonus in 1598. Meckels diverticulum is an anomaly derived from incomplete obliteration of omphalo-mesenteric duct. It is rarely seen in adults, with prevalence of male to female of 2:1. Complications associated with Meckels diverticulum are hemorrhage, inflammation and intestinal obstruction. We present to you a case of 17 year old male with unusual mechanism of small bowel obstruction due to Meckels diverticulum.

scholarly journals A Rare Case of Agenesis of Dorsal Pancreas

2012 ◽  
Vol 01 (01) ◽  
pp. 036-039
Author(s):  
Devi Jansirani D. ◽  
Shiva deep S. ◽  
Deepak Barathi S.
Keyword(s):  
Diabetes Mellitus ◽  
Computed Tomography ◽  
Congenital Anomaly ◽  
Rare Case ◽  
Splenic Vein ◽  
Uncinate Process ◽  
Present Patient ◽  
Rare Congenital Anomaly ◽  
Dorsal Pancreas ◽  
Agenesis Of Dorsal Pancreas

AbstractAgenesis of dorsal bud of the pancreas is an extremely rare congenital anomaly which results in absence of neck, body and tail of the adult pancreas. It may be associated with number of clinical features like diabetes mellitus, abdominal pain and chronic pancreatitis. Because of its rarity, we are reporting a case of agenesis of dorsal pancreas associated with early onset diabetes. Ultrasonography and Computed tomography showed absence of neck, body and tail of pancreas anterior to splenic vein and portal confluence; however head and uncinate process were normally present. Patient was thus diagnosed as agenesis of dorsal bud of pancreas.

scholarly journals Congenital femoral deficiency: a rare case report

2017 ◽  
Vol 4 (3) ◽  
pp. 1118
Author(s):  
Sadashiva B Ukkali ◽  
Khodaija Mahvish ◽  
Nazeer Jeergal
Keyword(s):  
Congenital Anomaly ◽  
Lower Limb ◽  
Rare Case ◽  
Detailed History ◽  
Rare Congenital Anomaly ◽  
Male Baby ◽  
Left Lower Limb ◽  
Rare Case Report ◽  
Type C ◽  
Proximal Femoral Focal Deficiency

Proximal femoral focal deficiency (PFFD) is a rare congenital anomaly. We present a case of an isolated unilateral congenital femoral deficiency that was born locally. A full-term male baby was brought to us with a complaint of short left lower limb. Examination revealed short left lower limb with absence of thigh. Detailed history was obtained and he was examined clinically as well as radiologically. He was diagnosed as a case of PFFD of type C. Proper evaluation and its management accordingly can help the patient to lead a socially and economically productive life. 

scholarly journals Ectopia Cordis: Two Different Cases with Literature Review

2018 ◽  
Vol 02 (02) ◽  
pp. 093-097
Author(s):  
Manoj Kumar Sahu ◽  
Mayank Yadav ◽  
Yatin Arora ◽  
Sarveshpal Singh ◽  
Velayoudam Devagourou ◽  
...  
Keyword(s):  
Congenital Anomaly ◽  
Literature Review ◽  
Treatment Option ◽  
High Mortality ◽  
Surgical Correction ◽  
Ectopia Cordis ◽  
Rare Congenital Anomaly ◽  
Final Treatment ◽  
Very High

AbstractEctopia cordis is a rare congenital anomaly with thoracic exteriorization of the heart. With few exceptions, it is universally fatal. Surgical correction is the only final treatment option for this defect but with a very high mortality. The authors present two cases of ectopia cordis, both were operated upon in urgent basis, and one baby survived.

scholarly journals Horseshoe adrenal gland associated with type 1 diastematomyelia in an asymptomatic adult

2021 ◽  
pp. 20200188
Author(s):  
Ruhaid Khurram ◽  
Faisal Ahmadi ◽  
Raunak Poonawala ◽  
Ahmad Samim Yasin
Keyword(s):  
Congenital Anomaly ◽  
Adrenal Gland ◽  
Inferior Vena Cava ◽  
Rare Case ◽  
Inferior Vena ◽  
Vena Cava ◽  
Rare Congenital Anomaly ◽  
Asymptomatic Adult ◽  
Neonates And Infants

A horseshoe adrenal gland is a rare congenital anomaly found almost exclusively in neonates and infants based on autopsy studies. It is a term used to describe a solitary adrenal gland situated in the midline, posterior to the inferior vena cava and abdominal aorta. To date, in the literature, there have been very few cases documented in adults and they have also been reported to be associated with other co-existing intra-abdominal, vascular and vertebral congenital anomalies. We describe a rare case of an asymptomatic adult patient who was incidentally found to have a horseshoe adrenal gland as well as a Type 1 diastematomyelia.

scholarly journals Ulnar Dimelia – a rare and neglected anomaly of upper extremity

2021 ◽  
Vol 5 (1) ◽  
pp. 26-29
Author(s):  
Yasir Salam Siddiqui ◽  
◽  
Mazhar Abbas ◽  
Nusra Rahman ◽  
Julfiqar Julfiqar
Keyword(s):  
Congenital Anomaly ◽  
Literature Review ◽  
Upper Extremity ◽  
Rare Congenital Anomaly ◽  
Male Baby ◽  
Staged Operations

Ulnar dimelia is a rare congenital anomaly of the upper extremity. The condition presents with double ulnae forearm and polydactyly with complete absence of radius bone and thumb. Clinically it presents not only as functional deformity but also as cosmetic deformity. The case presented here is of a one-and-a-half-year-old male baby, born with right side ulnar dimelia with no other musculoskeletal defect. We believe that the case presented here deserves reporting not only because of the rarity of the disease but also due to its difficult management requiring multiple staged operations and henceforth consequent neglect on the part of parents. An attempt is also made to do a brief literature review. Keywords: Ulnar dimelia; polydactyly; ulna; radius; thumb

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