Document Detail


Thymic sarcomatoid carcinoma with skeletal muscle differentiation: report of two cases, one with cytogenetic analysis.
MedLine Citation:
PMID:  11903597     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
AIMS: Malignant thymic tumour histologically resembling a soft tissue sarcoma is extremely rare and defined as sarcomatoid carcinoma in the recent World Health Organization (WHO) classification. We report two such cases in which the tumour cells showed a prominent rhabdomyoblastic differentiation and analyse whether these tumours retain an epithelial nature at least in part. METHODS AND RESULTS: One tumour occurred in a 51-year-old man (Case 1) and the other in a 40-year-old woman (Case 2). Microscopically, both tumours consisted essentially of two types of tumour cells: spindle and large round cells, with no apparent epithelial components. Osteosarcomatous small foci were also found in Case 2. Immunohistochemically, desmin and muscle-specific actin were positive in the majority of both types of tumour cells, whereas myogenin was predominant in the spindle cells and myoglobin in the large round cells. Some of both types of cells expressed cytokeratin with co-expression of myoglobin in the large round cells, but with no myogenin in the spindle cells. Some cytokeratin-positive spindle cells were also negative for desmin. Ultrastructural examination of a recurrent tumour in Case 2 revealed some epithelial features among the spindle cells. Cytogenetic study of the same tumour showed a complex abnormality including der(16)t(1;16)(q12;q12.1), an identical pattern previously reported in a case of thymic squamous cell carcinoma. CONCLUSIONS: The findings support the definition in the WHO classification of sarcomatoid carcinoma that includes purely sarcomatous tumour as in the present cases. Occurrence of this type of tumour may indicate a relationship between thymic epithelial cells and myoid cells and/or a potential for divergent differentiation in thymic epithelial tumours.
Authors:
T Eimoto; M Kitaoka; H Ogawa; H Niwa; T Murase; H Tateyama; H Inagaki; T Soji; H J Wang
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Publication Detail:
Type:  Case Reports; Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Histopathology     Volume:  40     ISSN:  0309-0167     ISO Abbreviation:  Histopathology     Publication Date:  2002 Jan 
Date Detail:
Created Date:  2002-03-20     Completed Date:  2002-05-15     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  7704136     Medline TA:  Histopathology     Country:  England    
Other Details:
Languages:  eng     Pagination:  46-57     Citation Subset:  IM    
Affiliation:
Department of Pathology, Nagoya City University School of Medicine, Kawasumi, Mizuho-ku, Nagoya 467-8601, Japan. teimoto@med.nagoya-cu.ac.jp
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MeSH Terms
Descriptor/Qualifier:
Adult
Carcinosarcoma / chemistry,  genetics,  secondary*
Chromosome Aberrations
Fatal Outcome
Female
Humans
Immunoenzyme Techniques
Karyotyping
Male
Middle Aged
Muscle, Skeletal / pathology*
Neoplasm Proteins / analysis
Neoplasm Recurrence, Local
Radiography, Thoracic
Thymus Neoplasms / chemistry,  genetics,  pathology*
Tomography, X-Ray Computed
Tumor Markers, Biological / analysis
Chemical
Reg. No./Substance:
0/Neoplasm Proteins; 0/Tumor Markers, Biological

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