Cholestasis Caused by Biliary Botryoid Sarcoma

Perisic, Vojislav N.; Er, Howard; Mihailovic, T; Vujanić, Gordan; Мilоvаnоvić, Drаgаn; Ivanovski, Petar

doi:10.1055/s-2008-1042498

Cited by 13 publications

(6 citation statements)

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“…Embryonal rhabdomyosarcoma (ERMS) of the CBD is a rare pathology among children. Symptoms of the onset of the disease are malaise, fever, and jaundice, as we have seen in our patient . Preoperative studies may reveal biliary cystic dilatation, leading to a diagnosis of congenital CC.…”

Section: Discussionsupporting

confidence: 60%

“…In ERMS of the biliary tract, tumor extension to the surrounding organs makes an anatomic resection almost impossible . This is the reason for the recommendation to carry out aggressive resections, such as pancreaticoduodenectomy, in these patients.…”

Section: Discussionmentioning

confidence: 99%

“…Symptoms of the onset of the disease are malaise, fever, and jaundice, as we have seen in our patient. [1][2][3][4][5][6][7][8][9][10][11][12] Preoperative studies may Abstract Embryonal rhabdomyosarcoma of the common bile duct is a very rare malignancy of childhood. The radiological appearance of the lesion is similar to that of congenital choledochal cyst if there is no local invasion to the adjacent tissues.…”

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confidence: 99%

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Embryonal rhabdomyosarcoma of the common bile duct mimicking choledochal cyst

Tireli¹,

Sander²,

Dervışoğlu

et al. 2005

J Hepatobiliary Pancreat Surg

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Embryonal rhabdomyosarcoma of the common bile duct is a very rare malignancy of childhood. The radiological appearance of the lesion is similar to that of congenital choledochal cyst if there is no local invasion to the adjacent tissues. The authors present a case of embryonal rhabdomyosarcoma of the common bile duct which was considered to be a congenital choledochal cyst preoperatively, and they discuss this very rare childhood tumor, with a brief survey of the literature. In conclusion, it is important to know that this rare tumor can simulate congenital choledochal cyst; it should be considered in the differential diagnosis of obstructive jaundice in children.

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Section: Discussionsupporting

confidence: 60%

Section: Discussionmentioning

confidence: 99%

mentioning

confidence: 99%

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Embryonal rhabdomyosarcoma of the common bile duct mimicking choledochal cyst

Tireli¹,

Sander²,

Dervışoğlu

et al. 2005

J Hepatobiliary Pancreat Surg

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“…(23%) [4][5][6][7][8] . Menos frecuentemente se puede originar en los miembros superiores e inferiores (17%) o en el tronco (8%).…”

Section: Discussionunclassified

Reporte de caso. Rabdomiosarcoma botrioides de la vía biliar

Lizcano¹,

Navarro²,

Avelino³

et al. 2016

Imagen Diagnóstica

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Recibido el 10 de marzo de 2015; aceptado el 7 de mayo de 2015 Disponible en Internet el 6 de noviembre de 2015 PALABRAS CLAVEQuiste de colédoco; Rabdomiosarcoma de la vía biliar Resumen El rabdomiosarcoma de la vía biliar es un tumor raro en niños. Tiene un pobre pronóstico, y representa alrededor del 8% de todos los cánceres en niños menores de 15 años. El sitio más comúnmente involucrado incluye cabeza y cuello (36%). Raramente se encuentra en víscera hueca: laringe, bronquios, intestino delgado y tracto biliar, y de manera frecuente se confunde con quiste de colédoco. A su vez, es el tumor más frecuente de la vía biliar: representa el 1% de todos los rabdomiosarcomas y aproximadamente el 0,04% de todos los tumores en niños. La apariencia radiológica es similar al quiste de colédoco cuando no existe extensión a órganos vecinos. En la tomografía axial computarizada la densidad de este tumor es menor que la del hígado y semeja un tumor quístico. El objetivo es reportar el caso Abstract Rhabdomyosarcoma (RMS) of the biliary tract is a rare tumour in children. It has a poor prognosis, and represents about 8% of all cancers in children younger than 15 years. The most commonly involved site includes head and neck, with 36%. Rarely found in viscera larynx, bronchi, small intestine and biliary tract, frequently confused with choledochal cysts, and in turn is the most common tumour of the bile duct, and represents 1% of all rhabdomyosarcomas, and about 0.04% of all tumours in children. The radiological appearance is similar to choledochal cyst when there is no extension to adjacent organs. In computed tomography, the density of this tumour is less than the liver and resembles a cystic tumour. The aim of the article is to report the cases in the 'Eva Samano Lopez Mateos' Children's Hospital.

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“…Paraneoplastic intrahepatic cholestasis has been described in several other malignancies including soft tissue sarcoma, medullary thyroid cancer, renal sarcoma, T-cell lymphoma, chronic lymphocytic leukemia, Hodgkin's disease (6)(7)(8)(9)(10)(11)(12). Although uncommon, reversible hepatic dysfunction in prostate cancer has been described in nine published cases (Table I) (1,(13)(14)(15)(16)(17)(18)(19)(20).…”

Section: Reversible Intrahepatic Cholestasis In Metastatic Prostatementioning

confidence: 99%

Reversible intrahepatic cholestasis in metastatic prostate cancer: An uncommon paraneoplastic syndrome

et al. 2018

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Abstract.As with other genitourinary malignancies, a variety of paraneoplastic syndromes have been revealed to occur in patients with prostate cancer. Stauffer's Syndrome is a well-described clinical syndrome which manifests via intrahepatic cholestasis in patients with renal cell carcinoma. Less common is intrahepatic cholestasis occurring in association with prostate cancer. The current case report discusses a 67-year-old man presenting with liver failure secondary to intrahepatic cholestasis co-existing with metastatic prostate adenocarcinoma. The patient's liver failure completely resolved with androgen-deprivation therapy suggesting an association between these two entities. The case report evaluates existing literature on this uncommon syndrome including the clinical presentation, natural history, and potential pathophysiology.

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Cholestasis Caused by Biliary Botryoid Sarcoma

Cited by 13 publications

References 0 publications

Embryonal rhabdomyosarcoma of the common bile duct mimicking choledochal cyst

Embryonal rhabdomyosarcoma of the common bile duct mimicking choledochal cyst

Reporte de caso. Rabdomiosarcoma botrioides de la vía biliar

Reversible intrahepatic cholestasis in metastatic prostate cancer: An uncommon paraneoplastic syndrome

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