30岁无症状女性低级别肺梭形细胞肿瘤:诊断困境:1例报告。

IF 0.8 Q4 RESPIRATORY SYSTEM Respirology Case Reports Pub Date : 2025-02-19 eCollection Date: 2025-02-01 DOI:10.1002/rcr2.70110
Jerica Eliesa Juarez, Albert Lim Rafanan, Matthew Go Yap
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引用次数: 0

摘要

肺梭形细胞癌是一种高度恶性的罕见的肉瘤样肺癌。这是一例无症状的30岁菲律宾女性,胸部x线片偶然发现肺结节。患者在2岁时被诊断为肾母细胞瘤,经S/P肾切除术后无复发记录。胸部CT示右上、中、下肺叶非钙化脂肪密度结节。正电子发射断层扫描(PET) CT扫描发现分叶状肺肿块具有低级别代谢活性。影像辅助胸外科手术右肺楔形切除。最后活检发现实质纤维上皮病变,由淡色梭形细胞组成。ER, SMA, desmin和caldesmon呈弥漫性阳性,与低级别梭形细胞肿瘤一致。基因检测显示CTNNB1 S45F亚克隆突变。未做化疗或放疗。全身重复PET CT显示肿块变小。
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Low Grade Pulmonary Spindle Cell Neoplasm in a 30-Year-Old Asymptomatic Female: A Diagnostic Dilemma: A Case Report.

Pulmonary spindle cell carcinoma is a highly malignant rare variant of sarcomatoid lung carcinomas. This is a case of an asymptomatic 30-year-old Filipino female with an incidental finding of pulmonary nodules on chest x-ray. Patient was diagnosed with Wilms tumor at the age of 2, S/P nephrectomy with no documented recurrence thereafter. Computed tomography (CT) chest scan showed non-calcified fat density nodules in her right upper, middle and lower lobe. A positron emission tomography (PET) CT scan identified lobulated pulmonary mass with low-grade metabolic activity. Video Assisted Thoracic Surgery with wedge resection of the right lung was done. Final biopsy noted fibroepithelial lesions in the parenchyma which composed of bland spindle cells. ER, SMA, desmin, and caldesmon were diffusely positive consistent with a low-grade spindle cell neoplasm. Genetic testing showed CTNNB1 S45F subclonal mutations. No chemotherapy nor radiotherapy were done. Repeat PET CT of the whole body showed a decrease in size of the mass.

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来源期刊
Respirology Case Reports
Respirology Case Reports RESPIRATORY SYSTEM-
CiteScore
1.40
自引率
0.00%
发文量
178
审稿时长
8 weeks
期刊介绍: Respirology Case Reports is an open-access online journal dedicated to the publication of original clinical case reports, case series, clinical images and clinical videos in all fields of respiratory medicine. The Journal encourages the international exchange between clinicians and researchers of experiences in diagnosing and treating uncommon diseases or diseases with unusual presentations. All manuscripts are peer-reviewed through a streamlined process that aims at providing a rapid turnaround time from submission to publication.
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