Rhabdomyoma of a Rare Type in a Child: Case Report and Literature Review

2001 ◽  
Vol 11 (1) ◽  
pp. 66-68 ◽  
Author(s):  
A. Cacciari ◽  
B. Predieri ◽  
M. Mordenti ◽  
P. L. Ceccarelli ◽  
A. Maiorana ◽  
...  
2015 ◽  
Vol 2 (1) ◽  
pp. 41-43
Author(s):  
Rajesh Kapila ◽  
Partap singh Verka ◽  
Radhe sham Garg ◽  
Mannan Ahmed

ABSTRACT Lateral swivel dislocation, a subtype pattern of dislocations occurring at mid tarsal joint is a rare type of injury. A medially or laterally directed force applied to the forefoot causes dislocation of the talonavicular joint but not subtalar joint. The calcaneum alongwith the remaining foot swivels on the intact interosseous talocalcaneal ligament. The present case report is a more rare lateral swivel type of dislocation of talonavicular joint in a 25-year-old male. The article also presents a comprehensive review of literature and management of such type of injuries of the hindfoot . How to cite this article Kapila R, Verka Ps, Garg Rs, Ahmed M. Lateral Swivel Dislocation of the Hindfoot: A Case Report and Literature Review. J Foot Ankle Surg (Asia-Pacific) 2015;2(1): 41-43.


2005 ◽  
Vol 91 (6) ◽  
pp. 552-554 ◽  
Author(s):  
Pierluigi Ballardini ◽  
Loretta Gulmini ◽  
Guido Margutti ◽  
Giorgio Lelli

Mesenteric fibromatosis is a rare type of desmoid tumor characterized by local aggressiveness and a tendency to relapse. In view of these characteristics it may be considered a low-grade fibrosarcoma. Camurati-Engelmann disease is a very rare form of bone dysplasia characterized by osteosclerosis of the diaphyses of the long bones. Here we describe the case of a male patient affected by these two rare diseases in association with chronic inflammatory intestinal disease.


2018 ◽  
Vol 52 ◽  
pp. 141-141
Author(s):  
E. di Pasquo ◽  
M. Kuleva ◽  
P. Sonigo ◽  
A. Millischer ◽  
D. Bremond-Gignac ◽  
...  

2018 ◽  
Vol 6 (11) ◽  
pp. 872-875
Author(s):  
FaisalEl mouhafid ◽  
◽  
Noureddine Njoumi ◽  
Mohamed Najih ◽  
Aziz Fadili ◽  
...  

2020 ◽  
Vol 48 (01) ◽  
pp. 061-065
Author(s):  
Margarida Areias Marques Miranda ◽  
Pedro Mota ◽  
Pedro Cardoso ◽  
Alexandre Pereira ◽  
Vânia Oliveira

AbstractMerkel Cell Carcinoma is a rare type of aggressive and often fatal neuroendocrine tumor of the skin.We report a clinical case of a 56-year-old female with a Merkel cell carcinoma on the left hand, without distant metastasis, treated with surgical excision of the lesion and radiotherapy.Based on this clinical case a research and review of the literature on this rare neoplasia was carried out.


2009 ◽  
Author(s):  
C. L. Khoo ◽  
L. Regina ◽  
S. R. K. Naik ◽  
S. Kang

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