scholarly journals LOW-GRADE FIBROMYXOID SARCOMA ADJACENT TO NEURAL STRUCTURE IN A 3 YEAR OLD GIRL: CASE REPORT AND REVIEW OF LITERATURE

2014 ◽  
pp. 1
Author(s):  
Salih Basat ◽  
Turgut Kayadibi ◽  
Ismail Akan ◽  
Mehmet Bozkurt
2018 ◽  
Vol 19 (1) ◽  
Author(s):  
Yali Yue ◽  
Yongkang Liu ◽  
Lina Song ◽  
Xiao Chen ◽  
Yaohui Wang ◽  
...  

2008 ◽  
Vol 47 (169) ◽  
Author(s):  
Arnab Ghosh ◽  
S Pradhan ◽  
R Swami ◽  
S R KC ◽  
O P Talwar

Here we describe a case of Reye syndrome diagnosed at postmortem liver biopsy of a three-year oldgirl who presented with vomiting, low grade fever for three days and loss of consciousness for 18hours. Clinically, the differential diagnoses were meningitis, encephalitis and septicemia. No historyof past illness or any drug ingestion including aspirin were present. Laboratory investigationsindicated a diagnosis of Reye syndrome. The child was given supportive treatment but died aftertwo days of admission and postmortem needle-biopsy of the liver showed microvesicular steatosisconsistent with Reye syndrome.Key words: Microvesicular steatosis, mitochondrial hepatopathy, Reye syndrome, Reye-like syndrome


2016 ◽  
Vol 9 (1) ◽  
pp. 85-89
Author(s):  
Svetlana A. Mateva ◽  
Margarita R. Nikolova ◽  
Alexandar V. Valkov ◽  
Margarita R. Nikolova

Summary Liposarcoma is one of the most common soft tissue sarcomas in adults with a relative incidence amongst other sarcomas ranging from 9.8% to 16%. It usually locates in the limbs and retroperitoneum. Primary liposarcomas of the larynx and hypopharynx are rare, comprising less than 20% of all head and neck liposarcomas. According to World Health Organization, these tumors are divided into four histologic types, and well-differentiated liposarcoma is the most common one. It is a tumor of low-grade malignancy that may recur locally, but does not metastasize. We present a case of laryngopharyngeal well- differentiated liposarcoma in an old patient with two previous removals. We also discuss recently published cases with this unusual location of liposarcoma.


2020 ◽  
Vol Volume 13 ◽  
pp. 6675-6680 ◽  
Author(s):  
Shuli Liu ◽  
Jinping Wang ◽  
Xue Luo ◽  
Xiaoman Li ◽  
Yuan Miao ◽  
...  

2020 ◽  
Vol 46 (9) ◽  
pp. 1921-1926
Author(s):  
Fatma Öz Atalay ◽  
Sevda Akyol ◽  
Önder Bozdogan

2016 ◽  
Vol 36 (7) ◽  
pp. 852-854 ◽  
Author(s):  
Jayanta Chatterjee ◽  
Stephanie Howden ◽  
Srdjan Saso ◽  
Sadaf Ghaem-Maghami ◽  
Angus McIndoe ◽  
...  

2010 ◽  
Vol 5 (1) ◽  
pp. 49 ◽  
Author(s):  
Christina Arnaoutoglou ◽  
Marios G. Lykissas ◽  
Ioannis D. Gelalis ◽  
Anna Batistatou ◽  
Anna Goussia ◽  
...  

2014 ◽  
Vol 57 (4) ◽  
pp. 162-164 ◽  
Author(s):  
Petr Kordač ◽  
Dimitar Hadži Nikolov ◽  
Katarína Smatanová ◽  
David Kalfeřt

Low-grade myofibroblastic sarcoma (LGMS) is a very rare, atypical myofibroblastic tumor with fibromatosis-like features with predilection mostly in head and neck region. LGMS occurs primarily in adult patients with a slight male predominance. Only few cases of LGMS affecting the larynx have been reported in literature to this date. We describe a case of low-grade myofibroblastic sarcoma of the larynx in a 40-year-old male patient. The clinicopathological characteristics, immunohistochemical findings and treatment are discussed.


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