29岁女性滑膜海绵状血管瘤伴关节旁血管瘤1例

Keykhosro Mardanpour , Mahtab Rahbar , Sourena Mardanpour , Mansour Rezaei
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摘要

滑膜血管瘤是一种罕见的良性血管畸形,最常影响膝关节,通常累及前腔室。组织病理学检查被认为是诊断滑膜血管瘤的金标准。手术切除,无论是每个关节镜或每个关节切开术,是治疗的选择。本研究报告了一名29岁女性,于2020年3月入院,主诉持续疼痛、肿胀和复发性关节病6个月,无创伤史。左膝正位平片及侧位平片未见异常。左膝超声显示关节内和髌上下囊的分叶状低回声病变。彩色多普勒成像显示病变内多支血管伴低速静脉血流。左膝磁共振成像显示关节窝内有不规则软组织肿块,沿股内侧肌(关节旁区)浸润髌上下囊约87 × 72 × 75 mm。滑膜积液和骨侵蚀明显。细针穿刺细胞学检查(FNAC)提示关节出血。在组织切除后立即从病变处进行切除活检和印迹细胞学检查。细胞学诊断符合良性血管肿瘤。组织学检查证实为滑膜血管瘤。滑膜血管瘤是一种罕见的良性肿瘤,起源于滑膜组织,常发生在青少年和年轻人身上。滑膜血管瘤常伴有邻近皮肤或深部软组织血管瘤。它是一种血管畸形,含有不同数量的脂肪、纤维和肌肉组织,以及血管中的血栓。目前,MRI已成为评估血管瘤的首选方式。最终诊断建立在组织学检查。治疗的选择是手术切除。结论滑膜血管瘤是一种罕见的疾病,临床症状不明确时应予以考虑。然而,滑膜血管瘤的早期诊断是充分治疗的基础。
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Synovial cavernous hemangioma with juxta-articular hemangioma in a 29-year old woman: A case report

Introduction

Synovial hemangiomas are a rare benign vascular malformation that most commonly affects the knee joint, usually involving the anterior compartment. Histopathology examination is considered the gold standard for the diagnosis of synovial hemangioma. Surgical excision, either done per arthroscopy or per arthrotomy, is the treatment of choice.

Presentation of case

This study presents a 29-year-old female admitted to our hospital in March 2020 who complained of continuous pain, swelling, and recurrent haemarthroses without a history of trauma for six months. The anteroposterior and lateral plain radiographs of the left knee showed no abnormality. An ultrasound of the left knee showed lobulated hypoechoic lesions in intra-articular and infra-suprapatellar pouches. Multiple vessels within the lesion with the low-velocity venous flow have appeared in color-Doppler imaging. Magnetic resonance imaging (MRI) of the left knee showed an irregular soft tissue mass in intra-articular fossa that infiltrating infra-suprapatellar pouches along to vastus medialis muscle (juxta-articular areas) measuring about 87 × 72 × 75 mm. Synovial effusion and bone erosions were notable. Fine-needle aspiration cytology (FNAC) offered hemarthrosis.

The excisional biopsy obtained from the lesion and imprint cytology performed immediately after tissue removal. The cytologic diagnosis was compatible with a benign vascular neoplasm. The histologic exam confirmed synovial hemangioma.

Discussion

Synovial hemangioma is a rare benign tumor of vascular origin arising from synovium-lined tissues, and often affects adolescents and young adults. Synovial hemangioma is often associated with an adjacent cutaneous or deep soft tissue hemangioma. It is a vascular malformation that contains variable amounts of adipose, fibrous, and muscle tissue, as well as thrombi in the vessels. At present, MRI has become the modality of choice for the evaluation of hemangiomas. The final diagnosis established with the histologic examination. The choice treatment is surgical excision.

Conclusion

Although synovial hemangioma is a rare condition, be considered for non-specific clinical symptoms. However, an early diagnosis of synovial hemangioma is fundamental for adequate treatment.

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来源期刊
Human Pathology: Case Reports
Human Pathology: Case Reports Medicine-Pathology and Forensic Medicine
CiteScore
0.50
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0
审稿时长
16 weeks
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