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通过正电子发射断层成像检测到的罕见部位腱鞘巨细胞瘤与恶性肿瘤混淆:两例报告

Tenosynovial giant cell tumors in unusual locations detected by positron emission tomography imaging confused with malignant tumors: report of two cases.

作者信息

Takeuchi Akihiko, Yamamoto Norio, Hayashi Katsuhiro, Miwa Shinji, Takahira Masayuki, Fukui Kiyokazu, Oikawa Taku, Tsuchiya Hiroyuki

机构信息

Department of Orthopaedic Surgery, Graduate School of Medical Science, Kanazawa University, 13-1 Takara-machi, Kanazawa-shi, 920-8641, Ishikawa-ken, Japan.

Department of Ophthalmology, Graduate School of Medical Science, Kanazawa University, 13-1 Takara-machi, Kanazawa-shi, 920-8641, Ishikawa-ken, Japan.

出版信息

BMC Musculoskelet Disord. 2016 Apr 26;17:180. doi: 10.1186/s12891-016-1050-7.

Abstract

BACKGROUND

A tenosynovial giant cell tumor (T-GCT) is a benign synovial tumor arising from the synovium, bursae, or tendon sheath. It can be intra- or extra-articular and localized or diffuse. Diffuse T-GCT is considered as a locally aggressive. Positron emission tomography (PET) with fluorine-18 fluorodeoxyglucose with computed tomography (FDG PET/CT) is widely used to differentiate malignant from benign tumors and to detect distant metastasis. However, FDG PET/CT is limited by false-positive findings. In this study, we present two cases of T-GCT that developed in unusual locations and were confused with malignant tumors. The final diagnoses were histologically confirmed as T-GCTs.

CASE PRESENTATION

Case 1. A 45-year-old Japanese female presented with a left choroidal melanoma and an abnormal lesion adjacent to the first cervical (C1) lamina confirmed by a PET scan (maximum standardized uptake value [SUVmax] =9.9 g/ml). MRI of the neck also detected a soft tissue mass (14.6 × 7.7 × 7 mm) adjacent to the C1 lamina. The choroidal melanoma was treated by heavy carbon ion radiotherapy. Although the size of the C1 soft tissue tumor remained unchanged, a CT-guided biopsy confirmed the diagnosis of the neck mass as a T-GCT. Case 2. A 15-year-old Japanese male with multiple type 1 neurofibromatosis presented with a soft tissue mass (26.1 × 24.7 × 11.5 mm) of the extra-articular hip joint that was coincidentally detected by FDG PET/CT during examination of a mediastinal soft tissue mass. SUVmax of the mediastinal lesion was 2.6 g/ml and of the hip lesion was 12.8 g/ml. Thus, differentiation from a malignant tumor, such as a malignant peripheral nerve sheath tumor, was necessary. An open biopsy was performed, and the frozen section was diagnosed as T-GCT. The tumor was excised, and the final histological diagnosis confirmed T-GCT.

CONCLUSION

T-GCT can show high FDG uptake, which might be confused with malignancy. Although MRI findings and location might help in the diagnosis of a T-GCT, careful assessment is mandatory, especially in unusual locations.

摘要

背景

腱鞘巨细胞瘤(T-GCT)是一种起源于滑膜、滑囊或腱鞘的良性滑膜肿瘤。它可以位于关节内或关节外,可为局限性或弥漫性。弥漫性T-GCT被认为具有局部侵袭性。氟-18氟脱氧葡萄糖正电子发射断层扫描(PET)联合计算机断层扫描(FDG PET/CT)被广泛用于鉴别良恶性肿瘤及检测远处转移。然而,FDG PET/CT存在假阳性结果的局限性。在本研究中,我们报告了两例发生于不寻常部位且被误诊为恶性肿瘤的T-GCT病例。最终诊断经组织学证实为T-GCT。

病例介绍

病例1。一名45岁日本女性,患有左脉络膜黑色素瘤,PET扫描证实第一颈椎(C1)椎板旁有一异常病变(最大标准化摄取值[SUVmax]=9.9 g/ml)。颈部MRI也检测到C1椎板旁有一软组织肿块(14.6×7.7×7 mm)。脉络膜黑色素瘤接受了重离子放射治疗。尽管C1软组织肿瘤大小未变,但CT引导下活检确诊颈部肿块为T-GCT。病例2。一名15岁患有多发性1型神经纤维瘤病的日本男性,在检查纵隔软组织肿块时,FDG PET/CT偶然发现关节外髋关节处有一软组织肿块(26.1×24.7×11.5 mm)。纵隔病变的SUVmax为2.6 g/ml,髋关节病变的SUVmax为12.8 g/ml。因此,有必要与恶性肿瘤如恶性周围神经鞘瘤进行鉴别。进行了开放性活检,冰冻切片诊断为T-GCT。肿瘤被切除,最终组织学诊断证实为T-GCT。

结论

T-GCT可表现出高FDG摄取,这可能会与恶性肿瘤混淆。尽管MRI表现和部位可能有助于T-GCT的诊断,但必须进行仔细评估,尤其是在不寻常部位。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d67/4845480/e25d3b9ce42e/12891_2016_1050_Fig1_HTML.jpg

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