scholarly journals Localised biphasic mesothelioma with prominent myxoid stroma

Pathology ◽  
2021 ◽  
Author(s):  
Kaoru Ogawa ◽  
Noriko Kimura ◽  
Osamu Wakabayashi ◽  
Akira Kurose ◽  
Tadashi Hasegawa
Keyword(s):  
Rare Tumors ◽  
2012 ◽  
Vol 4 (3) ◽  
pp. 145-147 ◽  
Author(s):  
Kemal Behzatoğlu ◽  
Pelin Yildiz ◽  
Meltem Öznur ◽  
Erol R. Bozkurt

2006 ◽  
Vol 130 (9) ◽  
pp. 1358-1360 ◽  
Author(s):  
Stephen E. Vernon ◽  
Pablo A. Bejarano

Abstract Low-grade fibromyxoid sarcomas are uncommon deep soft tissue neoplasms first described by Evans in 1987. They exhibit a deceptively benign appearance, with a whorled or linear arrangement of spindle-shaped cells showing few to absent mitoses. A characteristic, but not specific, feature is the presence of areas of myxoid stroma. Recurrences are common, and late metastases have been recorded. A closely related but morphologically distinct tumor, the so-called hyalinizing spindle cell tumor with giant rosettes, has also been described; both neoplasms share the same cytogenetic abnormality, a balanced translocation resulting in a FUS/CREB3L2 fusion gene. Because of similar clinical behavior and the common cytogenetic abnormality, some authors prefer to consider both lesions as a single entity within the spectrum of low-grade sarcomas.


2005 ◽  
Vol 447 (5) ◽  
pp. 828-834 ◽  
Author(s):  
Jinru Shia ◽  
Jing Qin ◽  
Robert A. Erlandson ◽  
Roy King ◽  
Peter Illei ◽  
...  

Author(s):  
Aman Deep Raj ◽  
Murali Mohan Soma ◽  
S. P. Khajuria

Fibroepithelial stromal polyps are benign proliferations which are usually polypoid or pedunculated, and less than 5cm in size. They are generally single lesions but can be multiple during pregnancy. They can be polypoid or pedunculated and are usually solitary. Symptoms usually include bleeding, discharge and general discomfort with sensation of a mass. They typically have a central fibrovascular core and contain stellate and multinucleated stromal cells which are best seen beneath the surface epithelium. True myxoid stroma is absent. Although vulvovaginal fibroepithelial stromal polyps are well documented, a giant variant such as the one authors report here is rather rare. To the knowledge, present case is the largest fibroepithelial stromal polyp compared to others reported in the literature.


Author(s):  
Claudia Manini ◽  
José I. López

The overwhelming majority of bladder cancers are transitional cell carcinomas. Albeit mostly monotonous, carcinomas in the bladder may occasionally display a broad spectrum of histological features that should be recognized by pathologists because some of them represent a diagnostic problem and/or lead prognostic implications. Sometimes these features are focal in the context of conventional transitional cell carcinomas, but some others are generalized across the tumor making its recognition a challenge. For practical purposes, the review distributes the morphologic spectrum of changes in architectural and cytological. So, nested and large nested, micropapillary, myxoid stroma, small tubules and adenoma nephrogenic-like, microcystic, verrucous, and diffuse lymphoepithelioma-like, on one hand, and plasmacytoid, signet ring, basaloid-squamous, yolk-sac, trophoblastic, rhabdoid, lipid/lipoblastic, giant, clear, eosinophilic (oncocytoid), and sarcomatoid, on the other, are revisited. Key histological and immunohistochemical features useful in the differential diagnosis are mentioned. In selected cases, molecular data associated with the diagnosis, prognosis, and/or treatment are also included.


1994 ◽  
Vol 53 (1) ◽  
pp. 125-127 ◽  
Author(s):  
Ali M. Khalil ◽  
Daniel E. Nahhas ◽  
Nina S. Shabb ◽  
Fadi G. Shammas ◽  
Naji K. Aswad ◽  
...  

2016 ◽  
Vol 2016 ◽  
pp. 1-2
Author(s):  
Alex C. Tham ◽  
Nandini L. Chilagondanahalli ◽  
Manish M. Bundele ◽  
Jeevendra Kanagalingam

Oral neurothekeoma or nerve sheath myxoma is a rare benign oral tumour of nerve sheath origin. Historically, this tumour has been subclassified as myxoid (classic), mixed, or the cellular type, depending on the amount of myxoid stroma and cellularity. We present a case of oral neurothekeoma (mixed type) of the buccal mucosa. The tumour was completely excised. No recurrence was detected in the last 3 years after local excision.


2019 ◽  
Vol 27 (4) ◽  
pp. 446-449 ◽  
Author(s):  
Julia A. Ross ◽  
John Reith ◽  
Jaya Ruth Asirvatham

The differential diagnosis of myxoid lesions in the breast is broad and includes both benign and malignant entities. Assessment is particularly challenging on core biopsy specimens. Myofibroblastoma, initially thought to be more common in the adult male breast, is being recognized with increasing frequency in the female breast. The wider anatomic distribution of mammary-type myofibroblastoma has also become known, and many new morphological variants have been described. Though focal myxoid stroma may be noted in myofibroblastomas and occasional myofibroblastomas may contain atypical cells, there have been only 3 reports in the literature of myofibroblastomas with exclusive or predominantly myxoid stroma, and 2 of these contained atypical cells. We report another case of mammary myxoid myofibroblastoma with atypical cells in a 40-year-old woman and discuss the differential diagnoses of myxoid lesions in the breast.


BMC Cancer ◽  
2020 ◽  
Vol 20 (1) ◽  
Author(s):  
Takashi Okuyama ◽  
Shinichi Sameshima ◽  
Emiko Takeshita ◽  
Takashi Mitsui ◽  
Takuji Noro ◽  
...  

2012 ◽  
Vol 62 (2) ◽  
pp. 287-293 ◽  
Author(s):  
Stefano Sioletic ◽  
Paola Dal Cin ◽  
Christopher D M Fletcher ◽  
Jason L Hornick

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