Excisional treatment of renal hydatid cyst mimicking renal tumor with diode laser technique: A case report

Uçar, Murat; Akgül, Ahsen Karagözlü; Çelik, Fatih; Kılıç, Nizamettin

doi:10.1016/j.jpurol.2016.04.009

Cited by 6 publications

(7 citation statements)

References 14 publications

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“…[ 3 , 4 ]. There are several reported cases where the renal hydatid was misdiagnosed as a malignant tumor and a radical surgery was performed [ 4 - 6 ]. Bosniak renal cyst type 2F and 3 often resemble renal neoplasm and cause diagnostic dilemma ( Figure 4 , Table 1 ).…”

Section: Discussionmentioning

confidence: 99%

Isolated renal hydatid disease: laparoscopic approach to an uncommon entity (case report)

Kumar¹,

Singla²,

Ahmad³

et al. 2021

Pan Afr Med J

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Hydatidosis is a parasitic disease, endemic in various parts of the World. It frequently involves liver and lungs and, rarely, other organs as well. Isolated renal hydatidosis is a rare entity that accounts for less than 3% of all hydatid cases. Surgery remains the mainstay of treatment. We hereby report a case of isolated renal hydatid cyst involving left kidney that was managed by laparoscopic approach.

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Section: Discussionmentioning

confidence: 99%

Isolated renal hydatid disease: laparoscopic approach to an uncommon entity (case report)

Kumar¹,

Singla²,

Ahmad³

et al. 2021

Pan Afr Med J

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“…It usually presents as a locally advanced, high-grade carcinoma, with bone metastases[ 9 ]. In rare cases, these tumors can be large with a cystic appearance, such as in this case[ 3 , 11 ].…”

Section: Discussionmentioning

confidence: 99%

“…Current relevant literature is dominated mostly by case reports from small institutional cohort studies (Table 1 )[ 3 , 11 , 17 - 27 ]. The reported survival rate is controversial, being mostly reported as a median survival of 13-22 mo after diagnosis[ 5 , 9 ].…”

Section: Discussionmentioning

confidence: 99%

Cystic low-grade collecting duct renal carcinoma with liver compression — A challenging diagnosis and therapy: A case report

Fülöp

Gurzu

Jung

et al. 2020

WJGS

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BACKGROUND A collecting duct carcinoma is a very rare, malignant renal epithelial tumor. Distant metastases are present in one third of cases at the time of diagnosis. It is known to have a poor prognosis. CASE SUMMARY A 42-year-old male was sent to our surgery clinic for removal of a 119.2 mm × 108.3 mm encapsulated cystic mass, which was localized in the 8 th segment of the right liver lobe. The lesion was first identified on ultrasonography. A computed tomography scan confirmed the presence of a Bosniak type III cystic lesion, which affected the liver and convexity of the right kidney. Surgical intervention involved a right nephrectomy, with removal of the cystic mass. The patient was mobilized on the first postoperative day and was discharged after 7 d. The histological and immunohistochemical examination revealed a low-grade collecting duct renal carcinoma, which is a rare variant of papillary carcinoma, with low malignant potential. The patient did not receive chemotherapy and after 21 mo of follow-up, a radiological examination and laboratory analyses showed normal aspects. No relapse or other complications were reported. CONCLUSION To manage renal tumors properly, a correct histopathological diagnosis is crucial, as is early diagnosis and correct surgical treatment.

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“…Total excision consists of either wedge resection or partial nephrectomy and partial excision includes partial pericystectomy followed by capitonnage, re-approximation of the pericyst or marsupialization [4]. Renal sparing surgery by way of partial excision is possible and is the most adapted treatment whenever possible preceded by the injection of scolicidal agents into the cyst [2,4,12] No intervention is needed when the cyst walls are calcified [12]. Conventionally, it is recommended to start the patient on a course of oral albendazole after surgery [10].…”

Section: Discussionmentioning

confidence: 99%

Primary Renal Hydatid Cyst in Children: A Case Report

Jabloun

2019

RPN

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Echinococcosis is a prevalent zoonosis in endemic region in the world. Although Echinococcosis can be present in all parts of the human body, renal Echinococcosis is relatively uncommon compared to liver and lung localizations. Its diagnosis is sometimes problematic. There are no specific clinical symptoms or positive result in a routine laboratory analysis that will reliably confirm the diagnosis of renal echinococco. In this study, a primary right renal hydatic cyst which was found in a 7-year-old girl has been presented. The patient was treated successfully by open surgery in combination with postoperative chemotherapy with albendazole. Physicians should be aware of its clinical presentations and complications.

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Excisional treatment of renal hydatid cyst mimicking renal tumor with diode laser technique: A case report

Cited by 6 publications

References 14 publications

Isolated renal hydatid disease: laparoscopic approach to an uncommon entity (case report)

Isolated renal hydatid disease: laparoscopic approach to an uncommon entity (case report)

Cystic low-grade collecting duct renal carcinoma with liver compression — A challenging diagnosis and therapy: A case report

Primary Renal Hydatid Cyst in Children: A Case Report

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