肺及气管支气管树状颗粒细胞瘤:两例报告并文献复习。

IF 0.9 Q4 ONCOLOGY Rare Tumors Pub Date : 2023-01-01 DOI:10.1177/20363613231187822
Yoldez Houcine, Mouna Mlika, Chirine Moussa, Houda Rouis, Emna Brahem, Olfa Ismail, Sonia Maȃlej, Faouzi El Mezni
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引用次数: 0

摘要

肺颗粒细胞瘤(CGT)是一种罕见的肿瘤,起源于雪旺细胞。在气管支气管和肺部,它们仍然是一个诊断挑战。没有明确的标准来区分良性、非典型和恶性GCT。此外,其在呼吸道的真实频率尚不清楚。在这里,我们报告了2例支气管和肺部的gct。我们的目的是根据我们的病例和现有的文献,在一个大型的系统回顾中强调所有临床病理特征在气管支气管和肺树位置的罕见肿瘤的频率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Granular cell tumor of the lung and tracheobronchial tree: Two case-presentation with a review of the literature.

Pulmonary granular cells tumors (CGT) are rare tumors, that derive from Schwann cells. In the tracheobronchial and pulmonary tree, they remain a diagnostic challenge. There are no well-established criteria to differentiate between benign, atypical, and malignant GCT. Moreover, its real frequency in the respiratory tract is still unknown. Here, we represent 2 cases of bronchial and lung GCTs. We aim to highlight the frequency of all clinicopathological characteristics of this rare tumor in the tracheobronchial and pulmonary tree location based on our cases and the available literature in a large systematic review.

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来源期刊
Rare Tumors
Rare Tumors ONCOLOGY-
CiteScore
1.50
自引率
0.00%
发文量
15
审稿时长
15 weeks
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