Primary rhabdoid cancer of the ileum: A case report and review of the literature

Tóth, László; Nemes, Zoltán; Gomba, S; Asztalos, László; Molnar, Călin; András, Csilla; Szentirmay, Zoltán; Molnár, Péter

doi:10.1016/j.prp.2009.02.013

Cited by 15 publications

(40 citation statements)

References 24 publications

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“…GI tract localization is uncommon, and the prognosis of the affected patient is poor, because of the aggressive nature of this disease, which is characterized by early diffuse metastasis, with death generally occurring within 6 months from initial diagnosis [3]. As noted above, the majority of extrarenal rhabdoid tumors occur in children.…”

Section: Discussionmentioning

confidence: 99%

“…However, the authors of those studies did not perform an accurate analysis of all cases described in the literature. The last two reviews [3,4] were incomplete, because they did not describe two cases [7,8]. The mean age of the patients in the previous reports was 62.9 (range 52-81) years.…”

Section: Discussionmentioning

confidence: 99%

“…Adult forms are uncommon, and they are characterized by a poor prognosis [3]. The extrarenal variants are very aggressive, and have most often been located in the central nervous system, liver, soft tissues and colon [4].…”

Section: Introductionmentioning

confidence: 99%

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Malignant rhabdoid tumor of the small intestine in adults: a brief review of the literature and report of a case

et al. 2014

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A malignant rhabdoid tumor was first described as a subtype of Wilms tumor in 1978. The most frequent location of these tumors is the kidney, and they are common in childhood. The extrarenal localization of these tumors has been described mainly in the central nervous system (called atypical teratoid-rhabdoid tumors), liver, soft tissues and colon. Localization in the small intestine is uncommon and since the 1990s, only a few cases of malignant rhabdoid tumors in the small intestine have been reported. This tumor is very aggressive and the prognosis is poor. We herein present our personal experience with a rhabdoid tumor of the jejunum in a 76-year-old male, and also provide an analysis of the cases of malignant rhabdoid tumor of the small intestine previously described in the literature as for a brief review. We also compared the previous reports and our present case to try to identify prognostic factors.

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Section: Discussionmentioning

confidence: 99%

Section: Discussionmentioning

confidence: 99%

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Malignant rhabdoid tumor of the small intestine in adults: a brief review of the literature and report of a case

et al. 2014

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“…Malignant rhabdoid tumor, which first described in kidneys of infants and children, is a rare and highly aggressive neoplasm with very poor prognosis and unresponsiveness to conventional treatment [1][2][3]. This tumor has been reported at many other sites, such as central nervous system, spine, urinary bladder, thyroid, retroperitoneum, and so forth [1][2][3][4].…”

Section: Dear Editormentioning

confidence: 99%

“…This tumor has been reported at many other sites, such as central nervous system, spine, urinary bladder, thyroid, retroperitoneum, and so forth [1][2][3][4]. The gastrointestinal tract is even rarer site of this disease, only 22 cases of gastrointestinal malignant rhabdoid tumor have been previously described in literature, but only one case of rectal malignant rhabdoid tumor has been published to date [3].…”

Section: Dear Editormentioning

confidence: 99%

Malignant rhabdoid tumor of rectum: report of a case

Han

Liu

et al. 2010

Tech Coloproctol

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Malignant Extrarenal Rhabdoid tumor derived from the greater omentum: A case report and literature review

Shao,

Liu,

Wang

et al. 2024

Cancer Reports

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BackgroundMalignant extrarenal rhabdoid tumor (MERT) is a rare and highly metastatic tumor, which is more than 75% of patients dying within 6 months of initial diagnosis, and it often leads to misdiagnosis and delayed treatment.CaseThis paper reports a 16‐year‐old girl who presented with the chief complaint of acute abdominal pain. She underwent laparoscopic exploration and excisional biopsy, then pathological examination and immunohistochemistry revealed “extrarenal malignant rhabdomyoma.” One month after operation, she died of intra‐abdominal hemorrhage and multiple organ dysfunction.ConclusionMERT were often misdiagnosed and had a poor prognosis. The surgery and chemotherapy are usually beneficial to prolong the survival time of patients with MERT.

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Primary rhabdoid cancer of the ileum: A case report and review of the literature

Cited by 15 publications

References 24 publications

Malignant rhabdoid tumor of the small intestine in adults: a brief review of the literature and report of a case

Malignant rhabdoid tumor of the small intestine in adults: a brief review of the literature and report of a case

Malignant rhabdoid tumor of rectum: report of a case

Malignant Extrarenal Rhabdoid tumor derived from the greater omentum: A case report and literature review

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