Pancreatic pseudocyst masquerading as complex renal cystic disease – a case report

2014 ◽  
Vol 10 (3) ◽  
pp. 183-185
Author(s):  
Robert S Radcliffe ◽  
Agnes Lee ◽  
Simon T Williams
Keyword(s):  
Case Report ◽  
Pancreatic Pseudocyst ◽  
Cystic Disease ◽  
Renal Cystic Disease

Case Report. A case of unilateral renal cystic disease

Nephrology ◽  
2004 ◽  
Vol 9 (1) ◽  
pp. 31-32 ◽  
Author(s):  
SIK LEE ◽  
SUNG K PARK ◽  
SUNG K KANG ◽  
WON KIM
Keyword(s):  
Case Report ◽  
Cystic Disease ◽  
Renal Cystic Disease ◽  
Unilateral Renal Cystic Disease

scholarly journals UNILATERAL RENAL CYSTIC DISEASE : A CASE REPORT

2015 ◽  
Vol 4 (56) ◽  
pp. 9838-9841
Author(s):  
Anuradha Kapali ◽  
Raghuram P ◽  
Beerappa Jaipal ◽  
Sateesh Kumar Atmakuri ◽  
Ravindra Bangar
Keyword(s):  
Case Report ◽  
Cystic Disease ◽  
Renal Cystic Disease ◽  
Unilateral Renal Cystic Disease

scholarly journals Unilateral Renal Cystic Disease: A Case Report and Literature Review

2020 ◽  
Vol 8 (C) ◽  
pp. 160-163
Author(s):  
Darmadi Darmadi ◽  
Riska Habriel Ruslie ◽  
Nurlaila Qodrianti Siregar ◽  
Deli Theo ◽  
Syahrial Anas
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Specific Treatment ◽  
Family Health ◽  
Cystic Disease ◽  
Renal Cystic Disease ◽  
Health Related ◽  
Unilateral Renal Cystic Disease ◽  
Laboratory Examinations

BACKGROUND: URCD is a rare disease characterized by cysts with various sizes in a diffusely enlarged kidney without forming a distinct encapsulated mass. We present literature review and report a case of URCD in our center. The aim of the study was to report a case of unilateral renal cystic disease (URCD) in a 25-year-old female. CASE REPORT: The patient was a 25-year-old female. She came to emergency unit of Mitra Medika Amplas Hospital Medan, Indonesia, with dyspepsia associated symptoms. Physical examination and family health-related history were normal. Laboratory examinations and genetic evaluation showed no abnormalities. Ultrasonography examination revealed multiple cysts in her right kidney which was confirmed by computed tomography (CT) scan. The diagnosis of URCD was confirmed. No specific treatment was given and she was advised to do a routine follow-up. CONCLUSION: URCD may present with mild symptoms or even asymptomatic. Diagnosis is confirmed by imaging modalities with normal renal function and absence of genetic predisposition. The management is conservative. Routine follow-up is mandatory.

scholarly journals Lithium-induced Nephrotoxicity: A Case Report of Renal Cystic Disease Presenting as a Mass Lesion

2014 ◽  
Vol 2 (6) ◽  
pp. 186-188 ◽  
Author(s):  
Yvonne McCartney ◽  
Cliodhna Browne ◽  
Dilly M. Little ◽  
Christian Gulmann
Keyword(s):  
Case Report ◽  
Mass Lesion ◽  
Cystic Disease ◽  
Renal Cystic Disease

scholarly journals Congenital Giant Dysplastic Kidney Presenting as Respiratory Distress: A Case Report

2016 ◽  
Vol 6 (1) ◽  
pp. 15 ◽  
Author(s):  
Mahesh Kumar ◽  
Geeta Gathwala ◽  
KN Rattan ◽  
Sandeep Lather ◽  
Poonam Dalal
Keyword(s):  
Case Report ◽  
Respiratory Distress ◽  
Rare Case ◽  
Abdominal Mass ◽  
Multicystic Dysplastic Kidney ◽  
Cystic Disease ◽  
Respiratory Compromise ◽  
Renal Cystic Disease ◽  
Dysplastic Kidney ◽  
Common Causes

Multicystic dysplastic kidney (MCDK) is the most common form of renal cystic disease in children and is one of the most common causes of abdominal mass in infancy. Here in we are reporting a rare case of a large MCKD that caused respiratory compromise and the infant presented with respiratory distress.

Adventitial Cystic Disease of the External Iliac Artery - A Case Report

Swiss Surgery ◽  
2001 ◽  
Vol 7 (2) ◽  
pp. 90-94 ◽  
Author(s):  
Heim ◽  
Rosso
Keyword(s):  
Case Report ◽  
Iliac Artery ◽  
External Iliac Artery ◽  
Cystic Disease ◽  
Adventitial Cystic Disease ◽  
Präoperative Abklärung

Die zystische Degeneration der Adventitia (ZAD) in der A.iliaca externa ist mit zehn in der Literatur beschriebenen Fällen ein seltenes Phänomen. Eine rasch auftretende, einseitige Ischämiesymptomatik bei jungen Patienten sollte daran denken lassen und eine erweiterte präoperative Abklärung zur Folge haben. Die klassische Therapie mit Gefässresektion und Veneninterponat wird seit jeher kontrovers diskutiert. Wir berichten über einen Fall mit rezidivfreiem Verlauf über drei Jahre nach Exarterektomie.

scholarly journals Is it always Wilms’ tumor? Localized cystic disease of the kidney in an infant. An extremely rare case report and review of the literature

2020 ◽  
Vol 12 (1) ◽  
Author(s):  
Christos Kaselas ◽  
Charikleia Demiri ◽  
Vasilios Mouravas ◽  
Eleni Koutra ◽  
Kleanthis Anastasiadis ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Wilms Tumor ◽  
Pediatric Population ◽  
Benign Disease ◽  
Cystic Disease ◽  
Proper Treatment ◽  
Review Of The Literature ◽  
Rare Case Report ◽  
Renal Malignancies

Localized Cystic Disease of the Kidney (LCDK) is an extremely rare benign disease in pediatric population. Although its management is conservative and generally requires no treatment, the unfamiliarity with the disease can expose such patients to misdiagnosis as renal malignancies or uncertainty for proper treatment. We report such a case in an infant and review the current literature.

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