Zobrazeno 1 - 10
of 17 504
pro vyhledávání: '"11"'
Autor:
Hidekazu Nishizawa, Ryoma Kurahashi, Yoji Nagashima, Mitsuko Furuya, Ikuma Kato, Yoshiki Mikami, Masaya Baba, Masatoshi Eto, Tomomi Kamba, Yumi Honda
Publikováno v:
IJU Case Reports
Introduction Definitive diagnosis of translocation renal cell carcinoma is challenging. We herein experienced a case of translocation(6;11) renal cell carcinoma, successfully diagnosed by using fluorescence in situ hybridization. Case presentation Du
Publikováno v:
Histopathology. Wiley
Histopathology
Histopathology
Aims Primary intraosseous rhabdomyosarcoma (RMS) is a rare entity defined by EWSR1/FUS-TFCP2 or, less commonly, MEIS1-NCOA2 fusions. The lesions often show a hybrid spindle and epithelioid phenotype, frequently coexpress myogenic markers, ALK, and cy
Autor:
Roido Manavaki, Frank H. Hezemans, Young T. Hong, James B. Rowe, George Savulich, Maura Malpetti, Tim D. Fryer, John T. O'Brien, Julie Wiggins, Jonathan P. Coles, Selena Milicevic Sephton, Istvan Boros, Negin Holland, P. Simon Jones, Franklin I. Aigbirhio
Publikováno v:
Mov Disord
BACKGROUND: Synaptic loss is a prominent and early feature of many neurodegenerative diseases. OBJECTIVES: We tested the hypothesis that synaptic density is reduced in the primary tauopathies of progressive supranuclear palsy (PSP) (Richardson's synd
Publikováno v:
International Journal of Gynecological Pathology. 39:296-300
We report a 55-yr-old woman who presented with bilateral ovarian masses, 11 yr after hysterectomy for superficially invasive stage IA1 cervical adenocarcinoma of usual (human papillomavirus-associated) type. The bilateral ovarian tumors were composed
Autor:
Pilar González-Peramato, José M. Viguer, Pilar López-Ferrer, Carlos H. Gordillo, Ana Margarita Rodríguez-García, José A. Jiménez-Heffernan, Patricia Muñoz-Hernández, Blanca Vicandi
Publikováno v:
Diagnostic Cytopathology. 48:1013-1020
Background Polymorphous adenocarcinoma (PAC) is a rare malignant tumor of the minor salivary glands. It has an infiltrative growth, variable architectural patterns, neurotropism and cellular monomorphism. Approximately 75% of the cases show a specifi
Publikováno v:
International Journal of Surgical Pathology. 28:609-615
Mesenchymal lesions of the gastrointestinal tract are generally uncommon compared with epithelial derived entities. Angiolipofibroma describes a rare gastrointestinal tract mesenchymal lesion composed of varied amounts of adipose tissue, fibrous tiss
Autor:
Hirokazu Furuya, Toru Iwaki, Naokazu Sasagasako, Satoshi O. Suzuki, Hiroyuki Honda, Shinichiro Mori, Takayuki Taniwaki, Hideomi Hamasaki
Publikováno v:
Neuropathology.
Spastic paraplegia type 11 (SPG11) is the most common autosomal recessive hereditary spastic paraplegia with thinning of the corpus callosum. Spatacsin, a protein encoded by the SPG11 gene, is associated with autophagy. SPG11 patients show spastic pa
Autor:
Tsutomu Ogata, Ho-Ming Luk, Akie Nakamura, Fai-Man Ivan Lo, Shinichiro Sano, Keiko Matsubara, Masayo Kagami
Publikováno v:
American Journal of Medical Genetics. Part a
Autor:
Keisuke Goto, Takuma Oishi, Masaru Tanaka, Kohei Ogawa, Keiichiro Honma, Yoji Kukita, Haruto Nishida, Toshihiro Takai, Taiki Isei, Tsunekazu Hishima
Publikováno v:
HistopathologyReferences. 79(6)
AIMS The aim of this study was to determine the clinicopathological and genetic characteristics of axillary signet-ring cell/histiocytoid carcinoma (SRCHC) and the relationship between axillary SRCHC, eyelid SRCHC, and conventional apocrine carcinoma
Publikováno v:
The American journal of surgical pathology. 45(2)
Perivascular epithelioid cell neoplasms (PEComas) of the bladder are extremely rare, with ~30 case reports. A subset of PEComas contain TFE3 gene rearrangement, however, the distinct histomorphologic features of these translocation tumors has not bee