scholarly journals Giant Atypical Lipomatous Tumor of Posterior Mediastinum In Adolescent ：A Case Study and the Literature Review​

2020 ◽  
Author(s):  
Yang Zhang ◽  
Kai Chen ◽  
Qing-Rong Ma ◽  
Zhuang-Rong Huang ◽  
Shu-Guang Zhu
Keyword(s):  
Literature Review ◽  
Soft Tissue Sarcomas ◽  
Residual Tumor ◽  
Posterior Mediastinum ◽  
Diagnostic Methods ◽  
Atypical Lipomatous Tumor ◽  
Lipomatous Tumor ◽  
Complete Surgical Resection ◽  
Posterior Mediastinal ◽  
Mediastinal Liposarcoma

Abstract Background: It is usually common for liposarcoma as one of the soft tissue sarcomas to be found in adults, and the disease in children is the rare case. Case presentation: This article involves in a 14-year-old boy with a primary posterior mediastinal atypical lipomatous tumor. It also provides a literature review and summary for the disease with the aim of making the disease well learned, because of the absence of the uniform standards for the clinical features, diagnostic methods, best treatment methods, and clinical efficacy of the atypical lipomatous tumor.Conclusion: Complete surgical resection is the best method for the eradication of tumors. However, mediastinal liposarcoma can not be completely removed by surgery in some cases. For the treatment of residual tumor tissue, molecular inhibitors will be an important supplementary method for the treatment of liposarcoma in the future.

A Case of Atypical Lipomatous Tumor of the Lower Leg

2016 ◽  
Vol 78 (4) ◽  
pp. 379-381 ◽  
Author(s):  
Tatsuya OGAWA ◽  
Shijima TAGUCHI ◽  
Yoshio NAKAYAMA
Keyword(s):  
Lower Leg ◽  
Atypical Lipomatous Tumor ◽  
Lipomatous Tumor

scholarly journals A giant posterior mediastinal malignant peripheral nerve sheath tumor and benign neurofibroma in body surface: a case report

BMC Surgery ◽  
2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Yan Zhang ◽  
Hongfei Cai ◽  
Guangchao Lv ◽  
Yang Li
Keyword(s):  
Peripheral Nerve ◽  
Neurofibromatosis Type ◽  
Posterior Mediastinum ◽  
Pathological Examination ◽  
Nerve Sheath Tumor ◽  
Tumor Type ◽  
Peripheral Nerve Sheath Tumor ◽  
Nerve Tumor ◽  
Nerve Sheath ◽  
Posterior Mediastinal

Abstract Background Neurofibromatosis comprises neurofibromatosis type 1 (NF1) and type 2 (NF2). Major tumor type of NF1 are neurofibroma recognized as benign peripheral nerve tumor, malignant peripheral nerve sheath tumor (MPNST), and glioma. Case presentation We report a woman with a special condition, whose tumors in body surfaces were benign neurofibroma and tumors in posterior mediastinum are MPNST. The chest-enhanced CT suggested a round soft tissue density in posteriormediastium. The diagnosis was established by pathology and immunohistochemistry. A single-stage thoracoscopic mediastinal mass resection was performed. The whole operation went smoothly and the CT scan of lungs did not show relapse of tumor three months later. Conclusions The appearance of neurofibroma should draw particular attention to the possibility of developing MPNST. More careful imaging examinations should be carried out, and pathological examination could diagnose it.

Ocular Tuberculosis: Clinics, Diagnosis and Treatment (Literature Review)

The Eye ◽  
2021 ◽  
Vol 23 (2) ◽  
pp. 41-45
Author(s):  
O. E. Russkikh ◽  
N. Y. Nikolenko
Keyword(s):  
Literature Review ◽  
Diagnostic Methods ◽  
Diagnosis And Treatment ◽  
Ocular Tuberculosis ◽  
Treatment Regimens ◽  
The Russian Federation ◽  
Serious Disease ◽  
Suggested Classification

Ocular tuberculosis is a serious disease with a long recurrent course, often leading to a significant decrease in the visual functions and quality of life of patients as well as disability. In recent years, the incidence rate of the ocular tuberculosis in the Russian Federation has been declining: in 2016, according to a number of authors, its incidence amounted to 5.2%.Purpose. To systematize literature data on the topic of ocular tuberculosis.Materials and methods. We reviewed literature available on elibrary.ru, cyberleninka.ru websites and in “Clinical Ophthalmology” journal. Results. We suggested classification of the ocular tuberculosis lesions, analyzed modern diagnostic methods and treatment regimens and evaluated their effectiveness.Conclusions. Literature review revealed that in order to improve the quality of detection, diagnosis and treatment of ocular tuberculosis, joint efforts of ophthalmologists and phthisiologists as well as use of modern methods of tuberculinodiagnosis are essential.

scholarly journals Male urethral sarcoma: a case report and literature review

2015 ◽  
Vol 14 (1) ◽  
pp. 64-66
Author(s):  
Magno Almeida Nogueira ◽  
Guilherme Campelo Lopes dos Santos ◽  
Roberto Iglesias Lopes ◽  
Octavio Henrique Arcos Campos ◽  
Marcos Francisco Dall'Oglio ◽  
...  
Keyword(s):  
Case Report ◽  
Urinary Tract ◽  
Soft Tissue ◽  
Literature Review ◽  
Soft Tissue Sarcomas ◽  
Heterogeneous Group ◽  
Men 2

Urethral tumors are rare and aggressive. They usually affect men (2:1) and occur more commonly in white (85% of cases). Soft tissue sarcomas are a heterogeneous group of tumors that arise from embryonic mesoderm. It represents 1% of all cases of urinary tract malignancies and rarely primary affect the ureter. We report a case of male urethral sarcoma. To date, only two similar cases have been published in literature.

Pleomorphic fibroma and dermal atypical lipomatous tumor: are they related?

2013 ◽  
Vol 40 (4) ◽  
pp. 379-384 ◽  
Author(s):  
Tariq Al-Zaid ◽  
Wei-Lien Wang ◽  
Dolores Lopez-Terrada ◽  
Dina Lev ◽  
Jason L. Hornick ◽  
...  
Keyword(s):  
Atypical Lipomatous Tumor ◽  
Lipomatous Tumor

scholarly journals Dedifferentiated liposarcoma of the retroperitoneum with osteosarcomatous component

2012 ◽  
Vol 2 (2) ◽  
pp. 33 ◽  
Author(s):  
Wenbin Sun ◽  
Xiaoyan Sun ◽  
Dianbo Cao
Keyword(s):  
Adipose Tissue ◽  
Soft Tissue Sarcomas ◽  
Dedifferentiated Liposarcoma ◽  
Pathological Findings ◽  
Specific Tumor ◽  
Complete Surgical Resection ◽  
Calcified Tissue ◽  
Term Evaluation ◽  
Characteristic Features

Liposarcoma is one of the most common soft-tissue sarcomas and classified as five groups. Dedifferentiated liposarcoma includes multiple elements such as solid tissue, adipose tissue and calcified tissue, which is different from common liposarcoma in tissue constitue. Dedifferentiation to osteosarcoma is rarely described in the literature. We reported the radiological and pathological findings in a case of dedifferentiated liposarcoma with osteo-sarcomatous dedifferentiation in the retroperitoneum and discussed the characteristic features of this specific tumor. Complete surgical resection of the neoplasm is the only curative means, but establishing a prognosis remains a challenge for long-term evaluation.

scholarly journals Giant posterior mediastinal liposarcoma presenting as dysphagia: A clinico-radio-pathologic correlation

2014 ◽  
Vol 3 (2) ◽  
pp. 43
Author(s):  
SantoshP V Rai ◽  
Sharada Rai ◽  
Rameshchandra Sahoo ◽  
Preetham Acharya ◽  
Maryann Bokelo ◽  
...  
Keyword(s):  
Pathologic Correlation ◽  
Posterior Mediastinal ◽  
Mediastinal Liposarcoma

Chlamydial conjunctivitis: clinic, diagnosis, treatment (literature review)

2021 ◽  
pp. 102-106
Author(s):  
A.E. Babushkin ◽  
Keyword(s):  
Literature Review ◽  
Key Words ◽  
Systemic Treatment ◽  
Review Article ◽  
Diagnostic Methods ◽  
Clinical Forms ◽  
Chlamydial Infections

The review article addresses the practical aspects of chlamydial conjunctivitis. In particular, it summarizes the clinical forms, diagnostic methods, local and systemic treatment of chlamydial infections of the eyes, as well as the prevention of this disease. Key words: chlamydial conjunctivitis, clinic, diagnosis, treatment.

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