scholarly journals Congenital Anterior Urethrocutaneous Fistula: Report of Three Cases

2018 ◽  
Vol 9 (2) ◽  
pp. 9 ◽  
Author(s):  
Akash Bihari Pati ◽  
Santosh Kumar Mahallik ◽  
Bikasha Bihary Tripathy ◽  
Manoj Kumar Mohanty
Keyword(s):  
Treatment Strategy ◽  
Postoperative Outcome ◽  
Rare Entity ◽  
Urethrocutaneous Fistula

The Congenital anterior urethrocutaneous fistula is a rare entity with varied anatomic configurations. In this report, we present three different varieties of congenital anterior urethrocutaneous fistula. The anterior urethrocutaneous fistula was associated with no urethra, hypoplastic urethra, and normal urethra, distal to fistula, 1 in each patient. Each required a different treatment strategy. Postoperative outcome was good in all cases.

scholarly journals Urethrocutaneous fistula mimicking vesicocutaneous fistula: a rare entity

2017 ◽  
pp. bcr-2017-219637
Author(s):  
Ruchir Aeron ◽  
Apul Goel ◽  
Ashok Kumar Sokhal ◽  
Sunny Goel
Keyword(s):  
Rare Entity ◽  
Urethrocutaneous Fistula ◽  
Vesicocutaneous Fistula

Congenital Megalourethra: A Rare Entity

2020 ◽  
Vol 5 (2) ◽  
Keyword(s):  
Reconstructive Surgery ◽  
Congenital Anomalies ◽  
Surgical Planning ◽  
Radiological Diagnosis ◽  
Rare Entity ◽  
Urethrocutaneous Fistula ◽  
Multiple Systems ◽  
Distal Obstruction ◽  
Congenital Megalourethra

Congenital megalourethra (CMU) is a dilatation of penile urethra without any distal obstruction. It occurs due to one or both corporal defect. About 80-100% cases of CMU are accompanied by multiple systems malformations which make the treatment more challenging. Cysto-urethrogram is necessary for radiological diagnosis and surgical planning. Depending on the type of the CMU and associated congenital anomalies, reduction urethroplasty or major reconstructive surgery is fashioned. We report a case of scaphoid variety of CMU in a 2 year child who was managed by reduction urethroplasty with additional dartos double breasting to prevent postoperative urethrocutaneous fistula (UCF).

1108: Treatment Strategy Improves the in Vivo Stone Comminution Efficiency and Reduces Renal Tissue Injury During Shock Wave Lithotripsy

2005 ◽  
Vol 173 (4S) ◽  
pp. 300-301
Author(s):  
Michaella E. Maloney ◽  
Pei Zhong ◽  
Charles G. Marguet ◽  
Yufeng F. Zhou ◽  
Jeffrey C. Sung ◽  
...  
Keyword(s):  
Shock Wave ◽  
Treatment Strategy ◽  
Shock Wave Lithotripsy ◽  
Tissue Injury ◽  
Renal Tissue

1115: The Effect of Treatment Strategy on Stone Comminution Efficiency in Shock Wave Lithotripsy

2004 ◽  
Vol 171 (4S) ◽  
pp. 294-294
Author(s):  
Yufeng Zhou ◽  
Charles G. Marguet ◽  
Michaella E. Maloney ◽  
Franklin H. Cocks ◽  
Glenn M. Preminger ◽  
...  
Keyword(s):  
Shock Wave ◽  
Treatment Strategy ◽  
Shock Wave Lithotripsy ◽  
Effect Of Treatment

A carotid bifurcation pseudoaneurysm treated endovascularly in a patient with irradiated neck

VASA ◽  
2019 ◽  
Vol 48 (2) ◽  
pp. 193-195
Author(s):  
Christiana Anastasiadou ◽  
Chrisostomos Maltezos ◽  
George Galyfos ◽  
Sotirios Giannakakis ◽  
Nikos Zannes ◽  
...  
Keyword(s):  
Carotid Artery ◽  
Endovascular Treatment ◽  
Carotid Bifurcation ◽  
Rare Entity ◽  
Artery Pseudoaneurysm

Abstract. A carotid artery pseudoaneurysm in an irradiated neck is a rare entity with possible devastating results and management should be multidisciplinary. We present a successful endovascular treatment of a late carotid artery pseudoaneurysm following patch endarterectomy and cervical radiotherapy.

Castleman's Disease Masquerading as Sigmoid Colon Tumor and Hodgkin Lymphoma

Swiss Surgery ◽  
2002 ◽  
Vol 8 (1) ◽  
pp. 7-10 ◽  
Author(s):  
Altinli ◽  
Pekmezci ◽  
Balkan ◽  
Somay ◽  
M. Akif Buyukbese ◽  
...  
Keyword(s):  
Lymph Nodes ◽  
Hodgkin Lymphoma ◽  
Sigmoid Colon ◽  
Castleman’S Disease ◽  
Malignant Potential ◽  
Colon Tumor ◽  
Rare Entity ◽  
Castleman's Disease ◽  
Mediastinal Lymph Nodes ◽  
Histologic Types

Castleman's disease is a benign lymphoid neoplasm first reported as hyperplasia of mediastinal lymph nodes. Some authors referred to the lesions as isolated tumors, described as a variant of Hodgkin's disease with a possibility of a malignant potential and others proposed that the lymphoid masses were of a hamartomatous nature. Three histologic variants and two clinical types of the disease have been described. The disease may occur in almost any area in which lymph nodes are normally found. The most common locations are thorax (63%), abdomen (11%) and axilla (4%). We report two separate histologic types of Castleman's disease which were rare in the literature, mimicking sigmoid colon tumor and Hodgkin lymphoma. The diagnostic and therapeutic aspects of this rare entity is discussed.

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