scholarly journals Complex treatment after pathohistological and immunohistochemical analysis in synchronous neoplasms - anorectal achromatic malignant melanoma and gastric extrapleural solitary fibrous tumor

2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Lena Marinova ◽  
Bistra Yordanova ◽  
Nikolay Evgeniev ◽  
Kremena Petrova
Author(s):  
Singh Harpal ◽  
Ramandeep Kaur ◽  
Ramandeep Kaur ◽  
Sunita Bhagat ◽  
Ramanpreet Kaur ◽  
...  

2016 ◽  
Vol 19 (1) ◽  
pp. 113
Author(s):  
Antonione Santos Bezerra Pinto ◽  
Vera Cavalcanti De Araújo ◽  
Fabrício Passador Santos ◽  
José Ferreira de Menezes Filho ◽  
Viviane Siqueira ◽  
...  

<p align="justify"><span style="color: #000000;"><span style="font-family: Arial, serif;"><span><span lang="en-US">A case of solitary fibrous tumor is reported. Solitary fibrous tumor is a rare neoplasia characterized by the proliferation of fusiform cells of mesenchymal origin accounting for at least </span></span></span></span><span style="font-family: Arial, serif;"><span><span lang="en-US">2% of all soft tissue tumors. In this present case, the initial diagnosis was salivary gland tumor because of the location in the hard palate. </span></span></span><span style="color: #000000;"><span style="font-family: Arial, serif;"><span><span lang="en-US">Histologically, the tumor was composed by conjunctive tissue with proliferation of oval and fusiform cells. The immunohistochemical analysis was positive for CD34 and CD99. The lesion was treated by surgical resection. The clinical, imaging, histological and immunohistochemical data are discussed in this study. </span></span></span></span></p><p lang="en-US" align="justify"> </p><p align="justify"><span style="color: #000000;"><span style="font-family: Arial, serif;"><span><span lang="en-US"><strong><span>Keywords</span></strong></span></span></span></span></p><p align="justify"><span style="font-family: Arial, serif;"><span><span lang="en-US">Solitary fibrous tumor; Oral cavity; Hard palate; Differential diagnosis.</span></span></span></p><p lang="en-US" align="justify"> </p>


Haigan ◽  
1998 ◽  
Vol 38 (2) ◽  
pp. 117-122 ◽  
Author(s):  
Futoshi Tsubokawa ◽  
Yukio Takeshima ◽  
Taijirou Sueda ◽  
Hiroo Shikata ◽  
Shinkichiro Yoshioka ◽  
...  

2016 ◽  
Vol 1 (2) ◽  
pp. 35-38
Author(s):  
Yuko Kobashi ◽  
◽  
Yohei Munetomo ◽  
Akira Baba ◽  
Shinji Yamazoe ◽  
...  

BMC Surgery ◽  
2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Liyun Wang ◽  
Jianbo Yu ◽  
Dongping Shu ◽  
Bin Huang ◽  
Yumin Wang ◽  
...  

Abstract Background Hemangiopericytoma (HPC), also known as solitary fibrous tumor (SFT), is a type of soft tissue sarcoma with a special aggressive behavior. The HPC/SFT is locally aggressive with possibility of late recurrence locally or distant extraneural metastasis. The most common location of this HPC/SFT is the lower extremities. The HPC/SFT in the central nervous system (CNS) is very rare, and compared with the brain, it is rarer in the spinal region. However, clinicians also lack an overall understanding of the diagnosis of HPC/SFT in the spinal cord. Case presentation In this study, we report a rare case of primary cervical spine HPC/SFT in a 53-year-old woman. Two to three weeks before admission, she experienced pain and numbness in her left upper extremity. After computerized tomography (CT) and magnetic resonance imaging (MRI), a gross total resection was performed. Obvious neurological improvement was observed postoperatively. The pain and numbness in the patient's left upper limb were relieved subsequently. We then reviewed the literature on HPC/SFT, such as its clinical presentation, imaging characteristics, treatment, and follow-up. Conclusions Diagnosis of HPC/SFT relies on magnetic resonance spectroscopy, enhanced CT, and MRI. Postoperative radiotherapy is strongly recommended to reduce the HPC/SFT recurrence. Immunohistochemical analysis can also help in the differential diagnosis. However; early and long-term follow-up is necessary for patients.


2015 ◽  
Vol 42 (4) ◽  
pp. 489 ◽  
Author(s):  
Dae Ho Kim ◽  
Jin Soo Lim ◽  
Ki-Taik Han ◽  
Min-Cheol Kim

2012 ◽  
Vol 78 (11) ◽  
pp. 487-489
Author(s):  
Giovanni Ramacciato ◽  
Francesco D'Angelo ◽  
Niccolò Petrucciani ◽  
Paolo Aurello ◽  
Matteo Ravaioli

2015 ◽  
Vol 105 (6) ◽  
pp. 557-559
Author(s):  
Charles A. Kean ◽  
Bridget R. Moore ◽  
Ashley M. Nettles ◽  
Richard P. Bui

Solitary fibrous tumors are uncommon mesenchymal neoplasms that were initially described as pleural tumors, but in recent years, numerous extrapleural sites have been reported. A solitary fibrous tumor is characterized as a circumscribed, painless mass with a patternless growth pattern, positive CD34 spindle-shaped cells, bcl-2, and dense keloidal collagen with areas of hypercellularity and hypocellularity. This case report describes a 55-year-old male veteran who presented with a rare manifestation of an extrapleural solitary fibrous tumor of the medial right hallux. Microscopic and immunohistochemical findings were consistent with the previously documented characteristics of solitary fibrous tumors. Complete surgical excision of the tumor is the treatment of choice.


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