Cardiac rhabdomyosarcoma: case report with review of clinical and pathologic features

1984 ◽  
Vol 51 (1) ◽  
pp. 83-88 ◽  
Author(s):  
R. C. Becker ◽  
R. E. Hobbs ◽  
N. B. Ratliff
Keyword(s):  
Case Report ◽  
Pathologic Features ◽  
Cardiac Rhabdomyosarcoma

scholarly journals Intraductal papillary mucinous tumor of bile ducts radiologic and pathologic features: a case report

Cases Journal ◽  
2008 ◽  
Vol 1 (1) ◽  
Author(s):  
Gianpaolo Carrafiello ◽  
Elena Bertolotti ◽  
Fausto Sessa ◽  
Tamara Cafaro ◽  
Gianlorenzo Dionigi ◽  
...  
Keyword(s):  
Case Report ◽  
Bile Ducts ◽  
Intraductal Papillary Mucinous Tumor ◽  
Mucinous Tumor ◽  
Pathologic Features

Dermatofibrosarcoma Protuberans Metastatic to the Lung. A Case Report

1992 ◽  
Vol 78 (1) ◽  
pp. 49-51 ◽  
Author(s):  
Prakash K. Patil ◽  
Snehal G. Patel ◽  
S. Krishnamurthy ◽  
Rajesh C. Mistry ◽  
Raman K. Deshpande ◽  
...  
Keyword(s):  
Case Report ◽  
World Literature ◽  
Dermatofibrosarcoma Protuberans ◽  
Primary Lesion ◽  
Wide Excision ◽  
Pathologic Features ◽  
The World ◽  
Long Term Follow Up

A case is presented of dermatofibrosarcoma protuberans of the gluteal region with metastasis to the lung appearing 7 years after wide excision of the primary lesion. The world literature is reviewed. The clinical and pathologic features of dermatofibrosarcoma are reviewed and treatment is discussed, with the aim of emphasizing the need for long-term follow-up examination of lymph nodes and for metastases following wide excision of these lesions.

A case report of primary cardiac rhabdomyosarcoma

1996 ◽  
Vol 8 (1) ◽  
pp. 8-8
Author(s):  
Zhang Zhenhua ◽  
Chen Ren
Keyword(s):  
Case Report ◽  
Cardiac Rhabdomyosarcoma

scholarly journals Primary Cardiac Rhabdomyosarcoma in a child -- A case report

2020 ◽  
Author(s):  
KRISHNA PRASAD MARAM ◽  
Vikram Kudumula ◽  
Dilip Ratti
Keyword(s):  
Case Report ◽  
Left Ventricle ◽  
Right Ventricle ◽  
Malignant Tumor ◽  
Right Atrium ◽  
Malignant Tumors ◽  
Benign Tumors ◽  
Cardiac Tumors ◽  
Cardiac Rhabdomyosarcoma ◽  
Primary Cardiac Tumors

Primary cardiac tumors are rare in children, usually consist of benign tumors like rhabdomyomas and fibromas that may spontaneously regress. Primary malignant tumors are extremely rare even in adults and very few paediatric cases were reported in literature. Rhabdomyosarcoma is a rare primary malignant tumor in children and most of the reported cases occur in right ventricle, left atrium and right atrium. We report a 15 month old child with primary rhabdomyosarcoma of left ventricle presenting in cardiac tamponade and circulatory failure.

Osteoblastoma

2010 ◽  
Vol 134 (10) ◽  
pp. 1460-1466 ◽  
Author(s):  
David R. Lucas
Keyword(s):  
Case Report ◽  
Bone Tumor ◽  
Bone Tumors ◽  
Differential Diagnoses ◽  
Benign Bone Tumor ◽  
Benign Bone Tumors ◽  
Pathologic Features ◽  
Clinicopathologic Findings

Abstract Osteoblastoma is a rare benign bone tumor. Although the histologic features in most cases are distinctive, there are various permutations that make the diagnosis challenging. It can mimic a variety of other benign bone tumors, but more importantly, distinguishing it from osteoblastoma-like osteosarcoma can be difficult. In this case report, I describe the clinicopathologic findings for a 13-year-old adolescent boy with T7 spinal osteoblastoma and review salient clinical, radiographic, and pathologic features of osteoblastoma, as well as the differential diagnoses.

Primary Cardiac Rhabdomyosarcoma of the Right Atrium: Case Report

2008 ◽  
Vol 11 (2) ◽  
pp. E117-E119 ◽  
Author(s):  
Onur Sokullu ◽  
Soner Sanioglu ◽  
Hayati Deniz ◽  
Umut Ayoglu ◽  
Ayca Ozgen ◽  
...  
Keyword(s):  
Case Report ◽  
Right Atrium ◽  
The Right ◽  
Cardiac Rhabdomyosarcoma

scholarly journals Acute Glomerulonephritis: Clinical and Pathologic Features (Case Report)

KIDNEYS ◽  
2016 ◽  
Vol 0 (1.15) ◽  
pp. 89
Author(s):  
O.O. Diadyk ◽  
L.H. Nekrasova ◽  
O.I. Taran ◽  
I.O. Siroshtanova ◽  
L.V. Kominko
Keyword(s):  
Case Report ◽  
Acute Glomerulonephritis ◽  
Pathologic Features

scholarly journals Nodular Fasciitis of the Orbit: A Case Report and Brief Review of the Literature

2011 ◽  
Vol 2011 ◽  
pp. 1-3 ◽  
Author(s):  
John E. Riffle ◽  
Andrea H. Prosser ◽  
Jeffery R. Lee ◽  
Julie J. Lynn
Keyword(s):  
Case Report ◽  
Medical Literature ◽  
Superficial Fascia ◽  
Nodular Fasciitis ◽  
Review Of The Literature ◽  
Mesenchymal Tumors ◽  
Pathologic Features ◽  
Orbital Region ◽  
Fibroblastic Proliferation

Nodular fasciitis is a benign, reactive, fibroblastic proliferation in which nodules most commonly develop in the subcutaneous or superficial fascia of the extremities. The occurrence of these growths in the orbital region is relatively rare. Our intent is to report another orbital case of this benign fibroproliferative tumor and to provide a brief review of the pertinent medical literature. The salient pathologic features of nodular fasciitis are summarized. The potential for the misdiagnosis of these benign mesenchymal tumors as a malignant sarcomatous neoplasm is discussed. It is important for ophthalmologists to be aware of this pathologic entity and its pseudosarcomatous appearance.

scholarly journals Biphasic Synovial Sarcoma of the Posterior Pharyngeal Wall: A Case Report

2005 ◽  
Vol 84 (5) ◽  
pp. 302-306 ◽  
Author(s):  
Frank O. Agada ◽  
Justin Murphy ◽  
Ravi Sharma ◽  
Laszlo Karsai ◽  
Nick D. Stafford
Keyword(s):  
Case Report ◽  
Head And Neck ◽  
Synovial Sarcoma ◽  
Neck Region ◽  
Posterior Pharyngeal Wall ◽  
Pharyngeal Wall ◽  
Head And Neck Region ◽  
Pathologic Features ◽  
Histopathologic Features

Synovial sarcoma is not common in the head and neck region. Because its histopathologic features are many and varied, it is often misdiagnosed. We report a case of biphasic synovial sarcoma of the posterior pharyngeal wall, and we discuss the clinical and pathologic features of this case.

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