scholarly journals A Rare Case of Low Grade, PAX-8 Positive Papillary Thymic Adenocarcinoma

2020 ◽  
Author(s):  
N. Aslam ◽  
M. Rai ◽  
C. Geller
Keyword(s):  
Rare Case ◽  
Low Grade ◽  
Thymic Adenocarcinoma

Multifocal low-grade central osteosarcoma: a rare case

2016 ◽  
Vol 45 (7) ◽  
pp. 997-1006 ◽  
Author(s):  
Richard Boyle ◽  
Bruno Giuffre ◽  
S. Fiona Bonar
Keyword(s):  
Rare Case ◽  
Low Grade

scholarly journals A rare case of low-grade fibromyxoid sarcoma with ossification which was radiologically detected as apparent calcification and histopathologically proven

2018 ◽  
Vol 12 ◽  
pp. 24-28
Author(s):  
Yasuaki Tsuchida ◽  
Yoshitane Tsukamoto ◽  
Hiroyuki Futani ◽  
Shunsuke Kumanishi ◽  
Takahiro Watanabe ◽  
...  
Keyword(s):  
Rare Case ◽  
Low Grade ◽  
Fibromyxoid Sarcoma

scholarly journals Pleomorphic xanthoastrocytoma at the pineal region: rare case report with successful surgical management

2021 ◽  
Vol 36 (1) ◽  
Author(s):  
Saraj Kumar Singh ◽  
Krishan Kumar Sharma ◽  
Tarun Kumar
Keyword(s):  
Surgical Management ◽  
Rare Case ◽  
Case Reports ◽  
Internal Capsule ◽  
Pleomorphic Xanthoastrocytoma ◽  
Pineal Region ◽  
Low Grade ◽  
Pineal Region Tumors ◽  
Pediatric Age Group ◽  
Rare Case Report

Abstract Background Pineal region tumors are commonly present in the pediatric age group. However, pleomorphic xanthoastrocytoma (PXA) is very rare at this region, and only few case reports have been reported till now in literature. Case presentation Here, we report a rare case of pineal region, juxta-thalamic, pleomorphic xanthoastrocytoma (PXA) in an 11-year-old male child. The child presented with severe headache after which MRI was done. It was suggestive of pineal region low-grade tumor. The patient was operated in Parkbench position with SCIT (supracerebellar approach) in a retractor-free manner. Gross total resection was done. However, the patient developed postoperative left-sided hemiparesis. It got improved in 1 month, and the patient became ambulatory. Histopathology came out as pleomorphic xanthoastrocytoma. Conclusion Surgical management should include careful resection near the internal capsule to avoid postoperative hemiparesis. Also, shunt should be delayed in the cystic cavity created by resection of tumor.

scholarly journals A rare case of low-grade appendiceal mucinous neoplasm within an incarcerated Amyand�s hernia

2017 ◽  
Vol 6 ◽  
pp. 13
Author(s):  
Diana Fernandes ◽  
Maria Olim Sousa ◽  
Ricardo Viveiros ◽  
Sara Silva ◽  
Susana N�brega ◽  
...  
Keyword(s):  
Rare Case ◽  
Low Grade ◽  
Mucinous Neoplasm

scholarly journals Low-Grade Endometrial Stromal Sarcoma in a 22-Year-Old Maiden Female: A Rare Case Report from Syria

2021 ◽  
Vol 2021 ◽  
pp. 1-4
Author(s):  
Lana Nseir ◽  
Georget Mansour ◽  
Junior Makhoul ◽  
Luna Skaf ◽  
Mohammad Ziad Dahhan ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Treatment Plan ◽  
Endometrial Stromal Sarcoma ◽  
Abnormal Uterine Bleeding ◽  
Low Grade ◽  
Stromal Sarcoma ◽  
Rapid Enlargement ◽  
Rare Case Report ◽  
Immunohistochemical Studies

Endometrial stromal sarcoma (ESS) is a rare and challenging type of endometrial tumor, constituting only about 0.2% of all uterine malignancies and occurring in women 42–58 years of age. ESS is usually misdiagnosed as leiomyoma. They both have nonspecific symptoms, which makes the diagnosis of ESS difficult to achieve. As the ESS is infrequently encountered, optimal management is quite debatable. Here, we report a rare case of a 22-year-old Syrian female who presented with abnormal uterine bleeding; the preoperative diagnosis suggested leiomyoma while histopathological and immunohistochemical studies confirmed the diagnosis of LG-ESS stage IIA. Therefore, the treatment plan was shifted from a conservative myomectomy to a total hysterectomy with both adnexa. The aim of this case report is to draw attention to this uncommon tumor at young age of patients as well as to have awareness of the necessity to suspect this diagnosis especially with the presentation of rapid enlargement of uterine leiomyoma.

scholarly journals Low-grade fibromyxoid sarcoma: A rare case in an unusual location

2020 ◽  
Vol 8 ◽  
pp. 2050313X2094431
Author(s):  
Diandra Perez ◽  
Ola El-Zammar ◽  
Brando Cobanov ◽  
Rana Naous
Keyword(s):  
Young Adults ◽  
Soft Tissue ◽  
Rare Case ◽  
Primary Site ◽  
Low Grade ◽  
Deep Soft Tissue ◽  
Unusual Location ◽  
Fibromyxoid Sarcoma ◽  
Intrathoracic Mass

Low-grade fibromyxoid sarcoma, also known as Evans tumor, is a low-grade sarcoma that most commonly arises in the deep soft tissue of the proximal extremities or trunk in young adults. It is very rare in the viscera as a primary site, with only a few cases reported in the literature. Here, we present a case of Evans tumor occurring in an unusual and rarely reported location; an intrathoracic mass arising from the diaphragmatic pleura.

scholarly journals Vulvar tuberculosis

2020 ◽  
Vol 13 (2) ◽  
pp. e232880
Author(s):  
Vishwajeet Singh ◽  
Gyanendra Singh ◽  
Rahul Janak Sinha ◽  
Suresh Babu
Keyword(s):  
Chronic Disease ◽  
Genital Tract ◽  
Rare Case ◽  
Low Grade ◽  
Fallopian Tubes ◽  
Genital Tuberculosis ◽  
Large Ulcer

Genital tuberculosis (TB) in women is a chronic disease with low-grade symptoms. Genital tract tuberculosis is usually secondary to extragenital TB. The fallopian tubes are most commonly affected, and along with endometrial involvement, it causes infertility in such patients. Involvement of the cervix and the vulva is very rare. We present one such rare case of vulvar tuberculosis presented with a large ulcer diagnosed on histopathology and treated with antitubercular chemotherapy.

Low-grade myofibroblastic sarcoma of the thoracic spine: report of an extreme rare case

2016 ◽  
Vol 31 (6) ◽  
pp. 731-733 ◽  
Author(s):  
Georgios F. Hadjigeorgiou ◽  
Vasilios Samaras ◽  
Vasilios Varsos
Keyword(s):  
Thoracic Spine ◽  
Rare Case ◽  
Low Grade ◽  
Myofibroblastic Sarcoma
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