scholarly journals Deep Aggressive Angiomyxoma of Pelvic Soft Tissue: A Rare Case Report

2012 ◽  
Vol 64 (6) ◽  
pp. 438-439 ◽  
Author(s):  
Anilkumar Sirasagi ◽  
Surekha Arakeri
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Rare Case ◽  
Aggressive Angiomyxoma ◽  
Rare Case Report

scholarly journals Solitary submandibular soft tissue osteochondroma: A rare case report

2021 ◽  
pp. 106074
Author(s):  
Abdulrahman Z. Nakshabandi ◽  
Ahamd F. Alomar ◽  
Moayad Baazeem ◽  
Abdulrahman Alosaimi ◽  
Ibrahim O. Bello
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Rare Case ◽  
Rare Case Report

Pulmonary Carcinosarcoma with Metastasis to Soft Tissue- A Rare Case Report

2019 ◽  
Author(s):  
M.R. Malekzadegan ◽  
K. Solanki ◽  
S.H.A. Pir ◽  
T.M. Arab ◽  
S. Chauhan ◽  
...  
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Rare Case ◽  
Rare Case Report ◽  
Pulmonary Carcinosarcoma

scholarly journals A maxillary ameloblastic fibrosarcoma tumor: a rare case report from Syria

2020 ◽  
Vol 2020 (8) ◽  
Author(s):  
Amjad Soltany ◽  
Ghazal Asaad ◽  
Rami Daher ◽  
Mouhannad Dayoub ◽  
Ali Khalil ◽  
...  
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Rare Case ◽  
Soft Tissue Sarcomas ◽  
Surgical Excision ◽  
Low Grade ◽  
Rare Case Report ◽  
Ameloblastic Fibrosarcoma ◽  
The Right

Abstract Ameloblastic fibrosarcoma (AFS) is a rare, aggressive malignant odontogenic tumor. AFS is seen most frequently in second and third decades of life. We are reporting a case of a low grade AFS in a 21-year-old male complaining of a painless swelling in the right side of the maxilla. The patient was treated with surgical excision followed by radiotherapy, which is considered the most effective approach for most of soft tissue sarcomas. AFS has a high-reported recurrence rate (up to 37%); therefore, long-term surveillance for recurrence is crucial.

scholarly journals Nasolabial hamartoma: a rare case report

2020 ◽  
Vol 6 (7) ◽  
pp. 1397
Author(s):  
D. Senthamarai Kannan ◽  
G. Soundara Rajan ◽  
Veerasigamani Narendrakumar ◽  
V. K. Sathiya
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Rare Case ◽  
Surgical Excision ◽  
The Body ◽  
Nasolabial Fold ◽  
Tissue Development ◽  
Inborn Errors ◽  
Complete Surgical Excision ◽  
Rare Case Report

<p class="abstract">Nasolabial cysts are rare, nonodontogenic soft tissue developmental cysts occur in the maxillary lip and nasal alar regions. Patients usually presents with an asymptomatic soft swelling with obliteration of the nasolabial fold. Due to it's origin from entrapped epithelium in an embryonic fusion plane developmentally, this cyst is considered to be a Hamartoma. Hamartomas are non-neoplastic malformations, or inborn errors of tissue development. They are characterized by an abnormal mixture of tissues indigenous to that area of the body. Complete surgical excision is the accepted method of treatment. This report aimed to present a case of nasolabial cyst hamartoma, which is rare in presentation.</p>

scholarly journals Histopathological Features of Deep Soft Tissue Epithelioid Angiosarcoma in the Lower Extremity: A Rare Case Report

2020 ◽  
Vol 21 ◽  
Author(s):  
Pham Nguyen Cuong ◽  
Nguyen Thanh Xuan ◽  
Pham Nhu Huy ◽  
Tran Nhu Tung ◽  
Nguyen Huu Son
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Lower Extremity ◽  
Rare Case ◽  
Deep Soft Tissue ◽  
Epithelioid Angiosarcoma ◽  
Histopathological Features ◽  
Rare Case Report

scholarly journals Bladder Chondrosarcoma in A Male: A Rare Case Report

2021 ◽  
Vol 57 (3) ◽  
pp. 256
Author(s):  
Muhammad Husni Tamrin ◽  
Wahjoe Djatisoesanto
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Soft Tissue Sarcoma ◽  
Rare Variant ◽  
Rare Case ◽  
Bladder Tumor ◽  
Histopathological Examination ◽  
Low Grade ◽  
Lower Abdomen ◽  
Rare Case Report

Chondrosarcoma is a rare variant of bladder tumor and one of the rare types of soft tissue sarcoma. This case happened on a 36-year-old male who complained of lumps in his lower abdomen, accompanied by difficulties in passing urine and painful urination, without hematuria. We performed TURBT and histopathological examination showed low-grade chondrosarcoma. The patient was diagnosed with low-grade bladder chondrosarcoma. The patient was treated for chemotherapy and radiotherapy. However, after undergoing one cycle of chemotherapy, the patient refused to continue the therapy.

scholarly journals Mucormycotic Osteomyelitis Involving the Maxilla: A Rare Case Report and Review of the Literature

2019 ◽  
Vol 2019 ◽  
pp. 1-6
Author(s):  
Rajesh Arani ◽  
S. N. H. Afsar Shareef ◽  
H. M. Khuthija Khanam
Keyword(s):  
Diabetes Mellitus ◽  
Case Report ◽  
Soft Tissue ◽  
Rare Case ◽  
Inflammatory Process ◽  
Review Of The Literature ◽  
The Past ◽  
Rare Case Report ◽  
Calcified Tissue ◽  
Fungal Osteomyelitis

Osteomyelitis is an inflammatory process of bone and marrow contents. These changes in bone are primarily seen in soft tissue followed by calcified tissue. It is an opportunistic infection due to the complication of some other conditions rendering the host susceptible to disease. Consequences of this infection range from draining tract to malignant transformation. Various etiological factors are involved in origin of the disease; among them, fungal origin is rare. Specific feature in fungal osteomyelitis is the involvement of maxillary sinus with a complaint of sinusitis associated with diabetes mellitus. Here, we discuss a case of osteomyelitis with fungal infection involving the maxilla. The patient is under medication for the past five years due to diabetes.

Soft tissue myoepithelial carcinoma of neck: A rare case report with review of literature

2014 ◽  
Vol 26 (4) ◽  
pp. 580-584 ◽  
Author(s):  
Niharika Swain ◽  
Shwetha V. Kumar ◽  
Jigna Pathak ◽  
Shilpa Patel
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Rare Case ◽  
Myoepithelial Carcinoma ◽  
Review Of Literature ◽  
Rare Case Report
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