The rare congenital anomaly of pulmonary sequestration experience and review of literature

2010 ◽  
Vol 26 (4) ◽  
pp. 251-254 ◽  
Author(s):  
Atilla Pekçolaklar ◽  
Necati Çitak ◽  
Muzaffer Metin ◽  
Abdülaziz Kök ◽  
Alper Çelikten ◽  
...  
Keyword(s):  
Congenital Anomaly ◽  
Pulmonary Sequestration ◽  
Review Of Literature ◽  
Rare Congenital Anomaly

scholarly journals Rare presentation of incomplete male urethral duplication: A case report and review of literature

2021 ◽  
Vol 9 (1) ◽  
pp. 292-296
Author(s):  
Orgeness J Mbwambo ◽  
Alex Mremi ◽  
Mohamed Mbarouk ◽  
Jasper Mbwambo ◽  
Frank Bright ◽  
...  
Keyword(s):  
Congenital Anomaly ◽  
Case Report ◽  
Postoperative Period ◽  
Surgical Removal ◽  
Urethral Duplication ◽  
Review Of Literature ◽  
Rare Presentation ◽  
Rare Congenital Anomaly ◽  
Accessory Urethra

Urethral duplication is a rare congenital anomaly affecting mainly males. Here, we report a case of urethral duplication in a 19 years old male presented as a scrotal sinus discharging pus for 1 year. Surgical removal of accessory urethra was done and postoperative period was uneventful.

scholarly journals Sirenomelia: A Case Report of a Rare Congenital Anomaly and Review of Literature

2016 ◽  
Vol 02 (01) ◽  
pp. 030-032
Author(s):  
Mohammad Khan ◽  
Pallavi Todase
Keyword(s):  
Congenital Anomaly ◽  
Umbilical Artery ◽  
Review Of Literature ◽  
Single Umbilical Artery ◽  
Rare Congenital Anomaly ◽  
Limb Bones ◽  
Mermaid Syndrome ◽  
First Case ◽  
Renal Abnormalities ◽  
Dysplastic Kidneys

AbstractSirenomelia, or the Mermaid Syndrome, is a very rare congenital anomaly. It is associated with varying degrees of fusion of lower limb bones, giving them the appearance of a “mermaid.” It is almost always associated with other birth defects, such as, renal abnormalities, genital anomalies, and cardiac anomalies. We report a case of sirenomelia associated with bilateral multicystic dysplastic kidneys along with bilateral hydronephrosis, severe oligohydramnios, single umbilical artery, absent anal opening, and absent genitals. To the best of our knowledge, this is the first case to be reported from our region.

scholarly journals Klippel-Feil Syndrome: A Review of Literature and Case Report

2018 ◽  
Vol 1 (1) ◽  
pp. 102-107
Author(s):  
H Mohammad ◽  
I T Annongu ◽  
D D Mue ◽  
D M Chia ◽  
R O Abah ◽  
...  
Keyword(s):  
Congenital Anomaly ◽  
Case Report ◽  
Review Of Literature ◽  
Rare Congenital Anomaly ◽  
Clinical Presentations ◽  
Complete History ◽  
Radiological Examinations

Though Klippel-Feil syndrome is a rare congenital anomaly and the clinical presentations are varied, a complete history, physical and radiological examinations may reveal the diagnosis.

scholarly journals Sirenomelia with Potter syndrome: a case report and review of literature

2019 ◽  
Vol 9 (1) ◽  
pp. 400
Author(s):  
Amrita Singh ◽  
Anupma Kumari
Keyword(s):  
Congenital Anomaly ◽  
Case Report ◽  
Prenatal Diagnosis ◽  
Lower Extremities ◽  
Rare Condition ◽  
Variable Degree ◽  
Review Of Literature ◽  
Rare Congenital Anomaly ◽  
Mermaid Syndrome ◽  
Vascular Steal

Sirenomelia or mermaid syndrome is a rare congenital anomaly characterized by variable degree of fusion of lower extremities. Awareness to this rare condition is important for prenatal diagnosis and prognosticating the fetus. The exact etiopathogenesis is still an area of research. Two pathogenic hypotheses are the vascular steal hypothesis and the defective blastogenesis hypothesis with exceptions reported in literature.

scholarly journals Complete Duplication of Collecting System in a Horseshoe Kidney Presenting with Recurrent Urinary Tract Infections: Report of an Exceedingly Rare Congenital Anomaly and Review of Literature

2011 ◽  
Vol 11 ◽  
pp. 1591-1596 ◽  
Author(s):  
Majid Mirzazadeh ◽  
Kyle A. Richards
Keyword(s):  
Congenital Anomaly ◽  
Urinary Tract ◽  
English Literature ◽  
Horseshoe Kidney ◽  
Review Of Literature ◽  
Ureteral Duplication ◽  
Rare Congenital Anomaly ◽  
Tract Infections ◽  
Complete Duplication ◽  
Collecting System

We report the fifth case in the English literature of a horseshoe kidney with a complete ureteral duplication. Our case is unique in that the previous four cases occurred in the presence of a ureterocele, whereas our patient lacked this anomaly. Further, our patient was managed conservatively, whereas the previous four patients were managed with surgery.

Retroperitoneal Pulmonary Sequestration: A Rare Congenital Anomaly in a 71-Year-Old Man

1994 ◽  
Vol 152 (6 Part 2) ◽  
pp. 2341-2343 ◽  
Author(s):  
Joel B. Nelson ◽  
Michael D. Blum ◽  
William A. Cook
Keyword(s):  
Congenital Anomaly ◽  
Pulmonary Sequestration ◽  
Rare Congenital Anomaly

scholarly journals A Patient with Intralobar Pulmonary Sequestration: A Rare Congenital Anomaly

2012 ◽  
Vol 20 (1) ◽  
pp. 99-102 ◽  
Author(s):  
Walter Beneduzzi Fiorotto ◽  
Leandro Zacarias ◽  
Marcio Ricardo dos Santos ◽  
Flavio Borges de Oliveira ◽  
Jamil Elias Dib Filho ◽  
...  
Keyword(s):  
Congenital Anomaly ◽  
Pulmonary Sequestration ◽  
Rare Congenital Anomaly ◽  
Intralobar Pulmonary Sequestration

scholarly journals Macrodystrophia Lipomatosa- A Rare Congenital Anomaly: A Case Report and Review of Literature

2016 ◽  
Vol 2 (5) ◽  
Author(s):  
Sanjay Kumar Tripathi ◽  
Saurav Narayan Nanda ◽  
Shalesh kumar ◽  
Nitin kumar Agrawal ◽  
Shaikh Muzammil Shiraz ◽  
...  
Keyword(s):  
Congenital Anomaly ◽  
Case Report ◽  
Review Of Literature ◽  
Rare Congenital Anomaly ◽  
Macrodystrophia Lipomatosa

scholarly journals Laparoscopic management of double gallbladder diagnosed intraoperatively: A case report and review of literature

2018 ◽  
Vol 87 (5-6) ◽  
Author(s):  
Jošt Kokalj ◽  
Yasmin Marianna Hunt
Keyword(s):  
Congenital Anomaly ◽  
Preoperative Diagnosis ◽  
Operative Procedure ◽  
Gall Stone ◽  
Review Of Literature ◽  
First Line ◽  
Rare Congenital Anomaly ◽  
Double Gallbladder ◽  
The Common ◽  
Gallbladder Removal

Double gallbladder is a rare congenital anomaly, which can present a challenge for the surgeon who performs laparoscopic cholecystectomies. The common first-line modality for screening in symptomatic gallbladder pathology is still ultrasonography, even though the accuracy is low. Preoperative diagnosis of this anomaly is not common as it is available in only 50 % of cases. Preoperative diagnosis and being acquainted with this anomaly decrease the possibility of injury to the biliary tract, the number of postoperative complications and the possible need for further surgical procedures.We present a case of double gallbladder which was diagnosed during the operative procedure. Based on ultrasonography screening, which showed a gall-stone in an unchanged gallbladder, a laparoscopic gallbladder removal was indicated. Despite the finding of a double gallbladder, the performance of laparoscopic gallblade removal was uneventful.

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