血管炎表现为肾脏、肺部和软组织多处肿块,类似恶性肿瘤

Shunhua Guo MD , Mary Ann R. Domingo MD , Qin Chang MD, PhD , Jordan K. Swensson MD
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引用次数: 0

摘要

我们报告一例肉芽肿病合并多血管炎(GPA)(韦格纳肉芽肿病),其表现为肾脏和肺叶以及颈部软组织的多发肿块病变,模仿恶性肿瘤。这名71岁的女性最初表现为右脚突然下垂,左小腿疼痛和右眼视力下降。她接受皮质类固醇治疗以诊断可能的颞动脉炎。类固醇逐渐减少到每天2 毫克几个月后,她出现了越来越多的疲劳、体重减轻和呼吸短促。CT扫描显示,左肺上叶肺质量病变(3.8 ×  2.4厘米),右中叶肺与胸膜扩展(3.4 ×  3.3厘米),和右叶低(1.1 ×  1.0厘米);右颈部(3.3 ×  2.6厘米),右肾(2.3 × 1.8 厘米)和左肾(2.0 ×  1.6厘米)。右股四头肌活检显示局灶性肉芽肿性炎症。肺活检显示坏死和形成不良的肉芽肿性炎症。肾肿块的活检表现为坏死性和非坏死性肉芽肿性炎症。在总共40个样本肾小球中未观察到新月形或坏死性肾小球病变。所有活检均未发现恶性肿瘤。c-ANCA阳性,PR3-ANCA抗体6.88 U/ml(正常0-0.90 U/ml)。她被诊断为肉芽肿病合并多血管炎,并接受大剂量皮质类固醇和利妥昔单抗治疗。8个月后随访,胸部x线及CT显示肿块病灶消退,肾功能稳定。该病例强调了血管炎的非典型临床表现,以及在面对多器官系统肿块病变时考虑这种可能性的鉴别诊断意义。活检对于正确诊断和及时适当治疗至关重要,对于避免不必要的手术切除也很重要。
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Vasculitis manifested with multiple mass lesions in kidneys, lungs and soft tissue, mimicking malignant tumors

We report a case of granulomatosis with polyangiitis (GPA) (Wegner's granulomatosis) who presented with multiple mass lesions in kidneys and lung lobes, as well as neck soft tissue, mimicking malignancies. This 71-year-old woman initially presented with sudden right foot drop, left calf pain and right eye vision loss. She was treated with corticosteroid for the diagnosis of possible temporal arteritis. Months after steroid was tapered to 2 mg per day, she developed increasing fatigue, weight loss, and shortness of breath. CT scan showed lung mass lesions in left upper lobe (3.8 × 2.4 cm), right mid lung with pleural extension (3.4 × 3.3 cm), and right lower lobe (1.1 × 1.0 cm); right neck (3.3 × 2.6 cm), right kidney (2.3 × 1.8 cm) and left kidney (2.0 × 1.6 cm). Right quadriceps muscle biopsy shows focal granulomatous inflammation. Lung biopsy showed necrotizing and poorly formed granulomatous inflammation. Biopsies of kidney mass lesions showed necrotizing and non-necrotizing granulomatous inflammation. No crescentic or necrotizing glomerular lesions were observed in the total 40 sampled glomeruli. No malignancy was identified in any of the biopsies. Her c-ANCA was found to be positive and PR3-ANCA antibody was 6.88 U/ml (normal 0–0.90 U/ml). She was diagnosed with granulomatosis with polyangiitis and treated with high dose corticosteroid and rituximab. Eight months later, follow-up showed resolved mass lesions by chest X-ray and CT and stable renal function. The case highlights the atypical clinical presentation of vasculitis and the significance of considering this possibility in differential diagnosis when confronting mass lesions present in multiple organ systems. Biopsy is critical for the correct diagnosis to initiate timely and appropriate treatment, and also important to avoid unnecessary surgical resection.

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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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0.00%
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0
审稿时长
16 weeks
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