scholarly journals An unusual complication following a shoulder relocation attempt in a case of Larsen syndrome: Deep soft tissue laceration of the arm

2021 ◽  
Vol 1 (1) ◽  
pp. 7-10
Author(s):  
Ahmet Burak Bilekli ◽  
Hakan Zeybek ◽  
Ali Aydilek ◽  
Yusuf Erdem
1980 ◽  
Vol 5 (4) ◽  
pp. 251-252 ◽  
Author(s):  
Andrea Meneghello ◽  
Massimo Bertoli ◽  
Gian Franco Romagnoli

1999 ◽  
Vol 48 (4) ◽  
pp. 1130-1132
Author(s):  
Tomoaki Horikawa ◽  
Kensuke Yonemura ◽  
Kimiaki Nishida ◽  
Toshitake Yakushiji ◽  
Teiji Kato ◽  
...  
Keyword(s):  

1995 ◽  
Vol 14 (11) ◽  
pp. 1002-1004 ◽  
Author(s):  
P. Kragsbjerg ◽  
T. Norén ◽  
B. Söderquist

2010 ◽  
Vol 124 (9) ◽  
pp. 1017-1020 ◽  
Author(s):  
A Toth ◽  
T Nemeth ◽  
A Szucs ◽  
Z Szollosi ◽  
I Sziklai

AbstractObjective:To describe the first published case of superficial angiomyxoma with an epithelial component occurring in the retropharynx.Method:Case report of a patient with swallowing difficulties caused by a rare case of superficial angiomyxoma in the retropharynx.Results:Superficial angiomyxoma is a distinct entity among the dermal myxomatous lesions. Superficial angiomyxoma is poorly circumscribed, and local recurrence is common unless the tumour is excised with clear margins. Distinctive histological features include a myxoid mass composed of spindle and stellate-shaped cells and occasional multinucleated cells. There is prominent vasculature and a mixed inflammatory infiltrate in the stroma, particularly by neutrophil polymorphs. Epithelial structures are seen in about one-third of cases. A case of retropharyngeal tumour with morphological features of superficial angiomyxoma is reported. The tumour cells, including multinucleated ones, were negative for soft tissue differentiation markers. The inflammatory cells included lymphocytes, histiocytes and neutrophil polymorphs.Conclusion:This case demonstrates that a cutaneous type of angiomyxoma with epithelial-lined structures can occur in deep soft tissue, such as the retropharynx.


2002 ◽  
Vol 126 (4) ◽  
pp. 468-470 ◽  
Author(s):  
Tetsuji Yamamoto ◽  
Rieko Minami ◽  
Chiho Ohbayashi ◽  
Mayumi Inaba

Abstract Epithelioid leiomyosarcoma in the external deep soft tissue is extremely rare. Most epithelioid leiomyosarcomas occur in the uterus. We present a case of epithelioid leiomyosarcoma occurring in the muscle of the thigh of a 78-year-old man. Histologically, the tumor predominantly consisted of round or polygonal cells arranged in sheets with a focal spindle cell component. Immunohistochemical analysis revealed that the tumor cells expressed vimentin, α-smooth muscle actin, and α-sarcomeric actin. The tumor was negative for desmin, S100 protein, glial fibrillary acidic protein, pan-keratin, epithelial membrane antigen, CAM 5.2, HMB-45, leukocyte common antigen, factor VIII–associated antigen, and CD34. Electron microscopically, some tumor cells contained abundant actin-type filaments in their cytoplasm.


2020 ◽  
Vol 8 ◽  
pp. 2050313X2094431
Author(s):  
Diandra Perez ◽  
Ola El-Zammar ◽  
Brando Cobanov ◽  
Rana Naous

Low-grade fibromyxoid sarcoma, also known as Evans tumor, is a low-grade sarcoma that most commonly arises in the deep soft tissue of the proximal extremities or trunk in young adults. It is very rare in the viscera as a primary site, with only a few cases reported in the literature. Here, we present a case of Evans tumor occurring in an unusual and rarely reported location; an intrathoracic mass arising from the diaphragmatic pleura.


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