Source:http://linkedlifedata.com/resource/pubmed/id/19633644
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rdf:type | |
lifeskim:mentions |
umls-concept:C0007589,
umls-concept:C0013216,
umls-concept:C0027651,
umls-concept:C0035412,
umls-concept:C0036525,
umls-concept:C0036679,
umls-concept:C0205070,
umls-concept:C0205453,
umls-concept:C0205615,
umls-concept:C0237868,
umls-concept:C0405581,
umls-concept:C0868928,
umls-concept:C1522484,
umls-concept:C2603343
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pubmed:issue |
10
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pubmed:dateCreated |
2009-9-30
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pubmed:abstractText |
To gain insight concerning prognosis, we investigated seven cases of post-chemotherapy retroperitoneal lymph-node dissections from patients with testicular germ-cell tumors that contained sizable nodules of differentiated skeletal muscle, but that lacked both a primitive cellular component and mitotic activity. The patients were 18-28 years old at the time of retroperitoneal lymph-node dissection. All had a previous non-seminomatous germ-cell tumor of the testis, five of which had a teratoma component. In one the testicular tumor had foci of embryonal rhabdomyosarcoma. The retroperitoneal lymph-node dissections were performed 0.2-4.7 years after orchiectomy, all following cisplatin-based chemotherapy, and contained rhabdomyomatous tumors that ranged from 0.8-5 cm. These consisted of nodular to diffuse aggregates of fetal-type rhabdomyocytes with central to peripheral nuclei and abundant, eosinophilic, fibrillary cytoplasm with occasional cross striations. Elongated myotubes with multiple nuclei in a common sarcoplasm occurred at least focally in all cases. Mild to moderate nuclear atypia, including nuclear enlargement and nucleolar prominence, was present, but mitotic activity, necrosis, and a primitive cellular component were absent. All but one retroperitoneal lymph-node dissection also contained other teratomatous elements. Follow-up in six patients showed three were disease free at 2.2-3.4 years; two developed recurrent teratoma at 1.3-3.7 years; and a sixth developed recurrent teratoma at 0.5 and 2 years, followed at 17 years by progressive tumor with elevated alpha-fetoprotein. No patient with available follow-up developed progressive sarcoma. We conclude that rhabdomyomatous tumors in retroperitoneal lymph-node dissection specimens after chemotherapy for metastatic testicular germ-cell tumors show clinical behavior similar to teratoma rather than rhabdomyosarcoma. We believe the most likely explanation for the finding of pure rhabdomyomatous tumors in this setting, a phenomenon sometimes termed 'cytodifferentiation,' is selective persistence of differentiated tumor cells because of chemotherapy.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1530-0285
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
22
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1361-6
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pubmed:meshHeading |
pubmed-meshheading:19633644-Adolescent,
pubmed-meshheading:19633644-Adult,
pubmed-meshheading:19633644-Antineoplastic Combined Chemotherapy Protocols,
pubmed-meshheading:19633644-Cell Differentiation,
pubmed-meshheading:19633644-Chemotherapy, Adjuvant,
pubmed-meshheading:19633644-Cisplatin,
pubmed-meshheading:19633644-Disease-Free Survival,
pubmed-meshheading:19633644-Humans,
pubmed-meshheading:19633644-Lymph Node Excision,
pubmed-meshheading:19633644-Lymph Nodes,
pubmed-meshheading:19633644-Lymphatic Metastasis,
pubmed-meshheading:19633644-Male,
pubmed-meshheading:19633644-Neoplasms, Germ Cell and Embryonal,
pubmed-meshheading:19633644-Orchiectomy,
pubmed-meshheading:19633644-Retrospective Studies,
pubmed-meshheading:19633644-Rhabdomyosarcoma, Embryonal,
pubmed-meshheading:19633644-Teratoma,
pubmed-meshheading:19633644-Testicular Neoplasms,
pubmed-meshheading:19633644-Time Factors,
pubmed-meshheading:19633644-Treatment Outcome,
pubmed-meshheading:19633644-Young Adult
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pubmed:year |
2009
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pubmed:articleTitle |
Differentiated rhabdomyomatous tumors after chemotherapy for metastatic testicular germ-cell tumors: a clinicopathological study of seven cases mandating separation from rhabdomyosarcoma.
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pubmed:affiliation |
Department of Pathology, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
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pubmed:publicationType |
Journal Article
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