scholarly journals Subcutaneous extraskeletal osteosarcoma of the foot: A case report

2021 ◽  
Vol 1 ◽  
pp. 25-27
Author(s):  
K. Sneha ◽  
Leena Dennis Joseph ◽  
M. Susruthan ◽  
R. Ramya
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Rare Variant ◽  
Binding Protein ◽  
Osteoblastic Differentiation ◽  
Bone Involvement ◽  
Nuclear Marker ◽  
Extraskeletal Osteosarcoma ◽  
Subcutaneous Tumor ◽  
Web Space

Extraskeletal osteosarcoma (ESOS) is a rare variant of osteosarcoma which occurs exclusively in the soft tissue without any bone involvement. Subcutaneous ESOS, in particular, is very rare and is seen in <10% of cases. Here, we report a case of a subcutaneous tumor in the fourth web space of the left foot in a 73-year-old man. The diagnosis of ESOS was made on histology and by immunohistochemical reactivity to special AT-rich sequence-binding protein 2 (SATB2), which is a sensitive, nuclear marker of osteoblastic differentiation. We present this case because of its rarity and the use of SATB2 immunohistochemistry to confirm the diagnosis.

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.

Case report: Infant with a Fast-growing Soft Tissue Tumor on the Thumb, Revealing a PLAG1-positive Connatal Lipoblastoma

2020 ◽  
Vol 232 (06) ◽  
pp. 285-288
Author(s):  
Susanne Deeg ◽  
Lucas Wessel ◽  
Richard Martel ◽  
Stefan Porubsky ◽  
Daniel Svoboda
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Local Recurrence ◽  
Soft Tissue Tumor ◽  
Soft Tissue Tumors ◽  
Diagnostic Specificity ◽  
Total Removal ◽  
Subcutaneous Tumor ◽  
Microsurgical Technique ◽  
The Right

AbstractAt the age of 4 months, an infant was presented to us with a nodular subcutaneous tumor on the right thumb measuring 2cm, already seen prenatally via ultrasound. An MRI in sedation performed at the age of 4.5 months had no diagnostic specificity. By a biopsy at the age of 5 months malignancy could be excluded. Finally at the age of 16 months the tumor which had meanwhile grown to a monstrous size (5 cm of diameter) could be entirely removed by microsurgical technique maintaining the integrity of all intrinsic structures. The diagnosis of myxoid lipoblastoma was confirmed. According to literature, Lipoblastomas often present as connatal rapid growing soft tissue tumors and are benign. Total removal is essential for avoiding a local recurrence.

scholarly journals Extraskeletal Osteosarcoma in the Thigh Recognized Following Acute Traumatic Injury: A Case Report and Review of the Literature

2020 ◽  
pp. 1-5
Author(s):  
Hope Jean Marie Vianney ◽  
Aboubacar S. Sangaré ◽  
Hope Jean Marie Vianney ◽  
Serge Ntungwanayo ◽  
J. Claude Sane
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Traumatic Injury ◽  
Left Thigh ◽  
Review Of The Literature ◽  
Extraskeletal Osteosarcoma ◽  
Instructive Case

Extraskeletal osteosarcoma is a rare mesenchymal malignancy arising in soft tissue that produces osteoid, neoplastic bone, or chondroid material without demonstrable attachments to bone or periosteum. We report an instructive case of extraskeletal osteosarcoma in a 42-year-old woman recognized following acute traumatic injury of her left thigh.

Soft Tissue Sarcoidosis of the Hand: A Case Report

1992 ◽  
Vol 17 (2) ◽  
pp. 230-231 ◽  
Author(s):  
D. C. GOTTLIEB ◽  
S. M. WENNER
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Soft Tissues ◽  
Bone Involvement ◽  
Systemic Sarcoidosis

A tumour of the hand may be the first manifestation of systemic sarcoidosis. In our patient, this mass involved only the soft tissues; more commonly, there is bone Involvement as well.

Inflammatory Myofibroblastic Tumor of Perineal Soft Tissue: A Case Report

2001 ◽  
Vol 45 (4) ◽  
pp. 417
Author(s):  
Jong Myeong Yang ◽  
Kyu Soon Kim ◽  
Soon Tae Kwon ◽  
Jong Chul Kim ◽  
Kyu Sang Song
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Inflammatory Myofibroblastic Tumor

Case Report: When all claims that it is necrotizing fasciitis but Point of care ultrasound (POCUS) proves the opposite!

POCUS Journal ◽  
2018 ◽  
Vol 3 (1) ◽  
pp. 13-14
Author(s):  
Hadiel Kaiyasah, MD, MRCS (Glasgow), ABHS-GS ◽  
Maryam Al Ali, MBBS
Keyword(s):  
Emergency Department ◽  
Critical Care ◽  
Case Report ◽  
Soft Tissue ◽  
Necrotizing Fasciitis ◽  
Soft Tissue Infection ◽  
Critical Care Unit ◽  
Point Of Care ◽  
Point Of Care Ultrasound ◽  
Soft Tissue Infections

Soft tissue ultrasound (ST-USS) has been shown to be of utmost importance in assessing patients with soft tissue infections in the emergency department or critical care unit. It aids in guiding the management of soft tissue infection based on the sonographic findings.

Myxoid atypical fibroxanthoma: a challenging diagnosis of a rare variant: Case report

2020 ◽  
pp. 399-403
Author(s):  
Nikolina Stavrinou ◽  
Stavroula Papadopoulou ◽  
Georgia Mitropoulou ◽  
Helen Trihia ◽  
Ioannis Provatas
Keyword(s):  
Case Report ◽  
Rare Variant ◽  
Atypical Fibroxanthoma
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