scholarly journals Fatal Course of Abdominal Neonatal Intestinal Fibrosarcoma

2019 ◽  
Vol 07 (01) ◽  
pp. e16-e19
Author(s):  
Béatrice Boutillier ◽  
Liesbeth Cardoen ◽  
Marianne Alison ◽  
Dominique Berrebi ◽  
Jonathan Rosenblatt ◽  
...  
Keyword(s):  
Soft Tissue ◽  
Small Bowel ◽  
Soft Tissue Tumor ◽  
Final Diagnosis ◽  
Childhood Cancers ◽  
Meconium Peritonitis ◽  
Neoplastic Lesion ◽  
Tumoral Lesion ◽  
Fatal Course ◽  
Extensive Surgery

AbstractInfantile fibrosarcoma (IFS) is a rare nonrhabdomyosarcoma soft tissue tumor and accounts for less than 1% of childhood cancers. Forty per cent are present at birth and only 10% of IFS occurs in the abdomen. Our case of neonatal fibrosarcoma presented as a distal small bowel stenosis complicated with meconium peritonitis. The diagnosis was by histology of the surgical resection. The diagnosis of IFS is challenging as there are no specific features of IFS on imaging. Any unexpected solid lesion should raise the suspicion of complicated bowel tumoral lesion. If a neoplastic lesion is suspected extensive, surgery may be postponed until the final diagnosis is made.

scholarly journals Paratesticular rhabdomyosarcoma - A case report

2019 ◽  
Vol 1 (2) ◽  
pp. 138-140
Author(s):  
Prakash Kayastha ◽  
Sharma Poudel ◽  
Rajan Mani Bhandari ◽  
Prem Raj Gyawali ◽  
Shova Banstola
Keyword(s):  
Case Report ◽  
Young Adult ◽  
Soft Tissue ◽  
Malignant Tumor ◽  
Soft Tissue Tumor ◽  
Clinical Presentation ◽  
Cell Tumor ◽  
Childhood Cancers ◽  
Scrotal Swelling

 Rhabdomyosarcoma is a malignant tumor of muscular origin. It comprises the most common soft tissue tumor in children accounting for approximately 5-8% of childhood cancers. Here we present a case of paratesticular rhabdomyosarcoma in a 13-year male child who was referred for ultrasonic examination (USG) to the department of radiology for evaluation of right scrotal swelling with pain for few months. Paratesticular rhabdomyosarcoma is a rare non germ cell tumor of scrotal sac in children and young adult/teens which can invade testis at presentation. We review the epidemiology, histology, clinical presentation, staging and prognosis of paratesticular rhabdomyosarcoma and discuss the role of radiology in their management.

scholarly journals Musculoskeletal Soft-Tissue Sarcoma: Quality Assessment of Initial MRI Reports Shows Frequent Deviation from ESSR Guidelines

Diagnostics ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 695
Author(s):  
Sebastian Weiss ◽  
Alexander Korthaus ◽  
Nora Baumann ◽  
Jin Yamamura ◽  
Alexander S. Spiro ◽  
...  
Keyword(s):  
Soft Tissue ◽  
Soft Tissue Sarcomas ◽  
Quality Criteria ◽  
Final Diagnosis ◽  
Tissue Mass ◽  
Musculoskeletal Radiology ◽  
Radiology Reports ◽  
Patients At Risk ◽  
Magnetic Resonance Imaging Mri ◽  
The Masses

Soft-tissue sarcomas (STS) are a rare subtype of soft-tissue mass and are frequently misinterpreted as benign lesions. Magnetic resonance imaging (MRI) is the primary recommended type of diagnostics. To assess the quality of primary radiology reports, we investigated whether recommended MRI report elements were included in compliance with European Society of Musculoskeletal Radiology (ESSR) guidelines. A total of 1107 patients were evaluated retrospectively, and 126 radiological reports on patients with malignant STS were assessed for ESSR quality criteria. One or more required sequences or planes were missing in 67% of the reports. In all 126 cases, the report recognized the mass as anomalous (100%). Sixty-eight percent of the reports mentioned signs of malignancy. The majority of reports (n = 109, 87%) articulated a suspected diagnosis, 32 of which showed a mismatch with the final diagnosis (25%). Thirty-two percent of the reports had a misinterpretation of the masses as benign. Benign misinterpretations were more common in masses smaller than 5 cm (65% vs. 27%). Thirty percent of the reports suggested tissue biopsy and 6% recommended referral to a sarcoma center. MRI reports showed frequent deviations from ESSR guidelines, and protocol guidelines were not routinely met. Deviations from standard protocol and reporting guidelines could put patients at risk for inadequate therapy.

scholarly journals A Case of Huge Soft Tissue Tumor of Thigh

2005 ◽  
Vol 54 (3) ◽  
pp. 578-581
Author(s):  
Takashi Maekawa ◽  
Toshitake Yakushiji ◽  
Yasuhiro Kawazoe ◽  
Katsuya Iwamoto ◽  
Hiroo Satou ◽  
...  
Keyword(s):  
Soft Tissue ◽  
Soft Tissue Tumor ◽  
Tissue Tumor

scholarly journals Subungual Glomus Tumor- Clinical Presentation And Treatment

2014 ◽  
Vol 3 (2) ◽  
pp. 45-48 ◽  
Author(s):  
Shyamal Chandra Debnath ◽  
Suman Kumar Roy ◽  
RR Kairy
Keyword(s):  
Soft Tissue ◽  
Soft Tissue Tumor ◽  
Clinical Presentation ◽  
Glomus Tumor ◽  
Rare Condition ◽  
Surgical Excision ◽  
Tissue Mass ◽  
Delay In Diagnosis ◽  
Nail Deformity

Glomus tumor is a rare condition and constitutes only 1 % of all soft tissue tumor of body. Glomus tumor is familiar for its unusual presentation and long standing symptoms due to delay in diagnosis. Authors have presented the clinical behavior and treatment of 7 patients with subungual soft tissue mass. Following surgical excision, all patients cured of symptoms, at the end of follow up, no recurrence occurred; post operative nail deformity was insignificant. DOI: http://dx.doi.org/10.3329/bdjps.v3i2.18250 Bangladesh Journal of Plastic Surgery July 2012, 3(2): 45-48

scholarly journals Angiomyofibroblastoma of the Foot: a Rare Soft Tissue Tumor at Unusual Site

2016 ◽  
Vol 8 (2) ◽  
pp. 210-213 ◽  
Author(s):  
Abhijeet Ashok Salunke ◽  
Yongsheng Chen ◽  
Victor KM Lee ◽  
Mark Edward Puhaindran
Keyword(s):  
Soft Tissue ◽  
Soft Tissue Tumor ◽  
Unusual Site ◽  
Tissue Tumor

Large Soft Tissue Tumor of the Chest Occurring After Trauma

1992 ◽  
Vol 85 (3) ◽  
pp. 317-318 ◽  
Author(s):  
SHAWN A. CHILLAG ◽  
ANTONIO R. CAFONCELLI ◽  
HO-HUANG CHANG ◽  
MILTON J. PLATA ◽  
DAVID ARTZ
Keyword(s):  
Soft Tissue ◽  
Soft Tissue Tumor ◽  
Tissue Tumor
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