Follicular Carcinoma Of The Thyroid Presenting As Distant Metastases: A Case Report And Review Of The Literature.

10.5580/2b25 ◽  
2012 ◽  
Vol 5 (1) ◽  
Keyword(s):  
Case Report ◽  
Follicular Carcinoma ◽  
Distant Metastases ◽  
Review Of The Literature

scholarly journals Thyroid-Like Follicular Carcinoma of the Kidney: One Case Report and Review of the Literature

2015 ◽  
Vol 144 (5) ◽  
pp. 796-804 ◽  
Author(s):  
Rahul Dawane ◽  
Alan Grindstaff ◽  
Anil V. Parwani ◽  
Timothy Brock ◽  
Wesley M. White ◽  
...  
Keyword(s):  
Case Report ◽  
Follicular Carcinoma ◽  
Review Of The Literature

scholarly journals Low-grade intracranial meningioma with bilateral pulmonary metastases incidentally detected postpartum: a case report and review of the literature

2021 ◽  
Vol 15 (1) ◽  
Author(s):  
Parviz Mardani ◽  
Arash Safarian ◽  
Anita Ashari ◽  
Sarina Pourjafar ◽  
Mohammad Hossein Anbardar ◽  
...  
Keyword(s):  
Case Report ◽  
Pulmonary Metastases ◽  
Lung Metastases ◽  
Rare Event ◽  
Distant Metastases ◽  
Intracranial Meningioma ◽  
Low Grade ◽  
Review Of The Literature ◽  
Case Presentation ◽  
Bilateral Lung

Abstract Introduction Meningiomas are the most commonly encountered intracranial tumors, usually showing indolent behavior. Extra-axial spreading and distant metastases are seldom detected in these tumors, and lung metastasis from a low-grade meningioma is a rare event. Case presentation This case report aimed to present the clinical, imaging, and pathological features of a 37-year-old Caucasian pregnant woman with bilateral lung metastases incidentally detected during preoperative workup ahead of surgery for a primary intracranial meningioma. The possible metastatic routes and risk factors of dissemination to the pulmonary circulation were discussed as well. Conclusion Metastasis must be considered in patients with intracranial meningiomas accompanied by venous sinus invasion and extension through the calvarium. Thorough paraclinical investigations are suggested in such cases.

Thyroid-Like Follicular Carcinoma of the Kidney With Extensive Sarcomatoid Differentiation: A Case Report and Review of the Literature

2019 ◽  
Vol 27 (6) ◽  
pp. 678-683 ◽  
Author(s):  
Taylor M. Jenkins ◽  
Jason Rosenbaum ◽  
Paul J. Zhang ◽  
Lauren E. Schwartz ◽  
Anupma Nayak ◽  
...  
Keyword(s):  
Case Report ◽  
Follicular Carcinoma ◽  
Good Prognosis ◽  
Molecular Profile ◽  
Review Of The Literature ◽  
Course Of Disease ◽  
Targeted Next Generation Sequencing ◽  
Poorly Differentiated ◽  
Generation Sequencing ◽  
Sarcomatoid Differentiation

Thyroid-like follicular carcinoma of the kidney (TLFCK) is an extremely rare primary renal malignancy that typically has an indolent course and good prognosis. Histologically, this tumor mimics follicular carcinoma of the thyroid; however, typical thyroid markers are negative. There are fewer than 40 cases reported in the literature, and thus, the prognosis and course of disease is not well understood. Sarcomatoid differentiation has never been reported in a case of TLFCK. We present a case of a 48-year-old woman with an aggressive TLFCK with extensive sarcomatoid differentiation and metastatic disease at presentation. We performed targeted next-generation sequencing of both the thyroid-like component and the poorly differentiated sarcomatoid component using our solid tumor panel to evaluate for any disease-associated mutations and to better understand the molecular profile of these tumors.

scholarly journals First case of bilateral, synchronous anaplastic variant of spermatocytic seminoma treated with radical orchifunicolectomy as single approach: Case report and review of the literature

2014 ◽  
Vol 86 (1) ◽  
pp. 41 ◽  
Author(s):  
Giorgio Gentile ◽  
Francesca Giunchi ◽  
Riccardo Schiavina ◽  
Alessandro Franceschelli ◽  
Marco Borghesi ◽  
...  
Keyword(s):  
Case Report ◽  
Distant Metastases ◽  
Testicular Neoplasm ◽  
Review Of The Literature ◽  
First Case ◽  
Spermatocytic Seminoma ◽  
Long Term Follow Up ◽  
Single Approach

Spermatocytic Seminoma (SS) is less common than the Classic variant, as its incidence ranges between 1.3% and 2.3% of all seminomas. Generally SS is diagnosed in men older than 50 years. The Anaplastic variant of Spermatocytic Seminoma is characterized by an earlier onset when compared to SS, but a benign behavior in spite of its histological patterns similar to Classic Seminoma. We reported the first case of bilateral, largest and synchronous Anaplastic Spermatocytic Seminoma, in a patient treated with radical orchifunicolectomy alone and with long-term follow-up. The currently available data show that Anaplastic SS reveals a clinically benign behavior, and no distant metastases have been reported so far. A close surveillance after surgery could be considered a valid option in the management of this rare testicular neoplasm.

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