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Department of Pathology, Charles University Hospital Plzen | 論文
- Diagnostic pitfall on the histological spectrum of adult-onset renal carcinoma associated with Xp11.2 translocations/TFE3 gene fusions
- Immunohistochemical application of D2-40 as basal cell marker in evaluating atypical small acinar proliferation of initial routine prostatic needle biopsy materials
- Chromophobe renal cell carcinoma : useful diagnostic application of imprint cytology and fluorescence in situ hybridization of chromosomes 10 and 21 in two cases of typical and eosinophilic variants
- Hybrid peripheral nerve sheath tumor of the nasal cavity showing schwannomatous, neurofibromatous, and perineuriomatous areas
- Chromosomal abnormalities of clear cell renal cell carcinoma : Frequent gain of chromosome 7
- Perivascular epithelioid cell tumor of the nasal cavity with TFE3 expression
- Renal angiomyoadenomatous tumor : fluorescence in situ hybridization
- Renal cell carcinoma with extensive clear cell change sharing characteristics of mucinous tubular and spindle cell carcinoma and papillary renal cell carcinoma
- Adult-onset renal cell carcinoma associated with Xp11.2 translocations/TFE3 gene fusion with smooth muscle stroma and abnormal vessels
- Carcinoid tumor of the renal pelvis : Consideration on the histogenesis
- Pancreatic undifferentiated carcinoma with osteoclast-like giant cells masquerading as (extra)gastrointestinal stromal tumor : Potential diagnostic pitfall
- Pigmented solid-pseudopapillary neoplasm of the pancreas
- Clear cell type of renal cell carcinoma with numerous hyaline globules : A diagnostic pitfall
- Acquired cystic disease-associated renal cell carcinoma with gain of chromosomes 3, 7, and 16, gain of chromosome X, and loss of chromosome Y
- Hybrid sclerosing adenosis and basal cell hyperplasia of the prostate