钇-90对胃肠道的损伤似乎主要局限于树脂微球,但可能在栓塞数年后发生

Michael M. Feely, R. Tondon, M. Gubbiotti, Kristen M. Stashek, N. Numbere, Aaron R. Huber, A. Sharma, B. Geller, Safia N. Salaria, Raul S. Gonzalez
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引用次数: 2

摘要

放射栓塞治疗利用钇-90 (Y90)浸渍树脂(SIR-Spheres)或玻璃(TheraSpheres)微球通过经动脉放射栓塞选择性靶向肝脏病变。偶有胃肠道损伤病例,继发于微球的非靶向递送,但缺乏大型描述性病理系列报道。我们从17例患者中鉴定了20例组织学证实的与Y90相关的粘膜损伤,并评估了相应的临床和病理后遗症。粘膜活检于Y90治疗后1至88个月(中位数:5个月)进行。大多数病例发生在胃(17.85%),其余病例发生在十二指肠。内镜下溃疡见于大多数病例(16.80%),粘膜红斑见于其余4例。组织学上,大多数(19.95%)病例显示圆形,深蓝色至紫色微球,直径4至30µm,与树脂微球一致。单个玻璃微球的案例显示出26µm的半透明珠子。14例(70%)有溃疡的组织学证据,6例(30%)有明显的血管内微球。异物巨细胞对微球的反应不常见(3例,15%)。此外,我们对784例连续接受Y90微球治疗的患者术后获得的所有胃肠道组织进行了回顾性回顾。3例患者(0.4%)在组织学检查中表现为树脂微球的存在。尽管大多数患者接受了玻璃放射栓塞(63,80%),但没有发现涉及玻璃基Y90的病例(P=0.0078)。这种增加的二次球传播风险可能与树脂微球比玻璃微球每次活性所需的颗粒数量增加有关。我们的结论是,在最初的肝脏靶向治疗后数年,胃肠道中可能会出现Y90微球,并且当存在时,通常与粘膜溃疡有关。这一发现在使用玻璃微球接受Y90放射栓塞的患者中不太可能遇到。
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Gastrointestinal Tract Injury by Yttrium-90 Appears Largely Restricted to Resin Microspheres But Can Occur Years After Embolization
Radioembolization therapy utilizes yttrium-90 (Y90) impregnated resin (SIR-Spheres) or glass (TheraSpheres) microspheres to selectively target hepatic lesions via transarterial radioembolization. Occasional cases of gastrointestinal tract injury, secondary to nontargeted delivery of microspheres, have been reported, but large descriptive pathology series are lacking. We identified 20 cases of histologically confirmed mucosal injury associated with Y90 from 17 patients and assessed the corresponding clinical and pathologic sequelae. The mucosal biopsies were obtained from 1 to 88 months following Y90 therapy (median: 5 mo). Most cases were gastric (17, 85%), while the remaining were duodenal. Endoscopic ulceration was seen in the majority of cases (16, 80%), and mucosal erythema in the remaining 4. Histologically, a majority (19, 95%) of cases showed rounded, dark blue to purple microspheres measuring 4 to 30 µm, consistent with resin microspheres. A single case with glass microspheres demonstrated 26 µm translucent beads. Histologic evidence of ulceration was appreciated in 14 (70%) cases, and the microspheres were clearly intravascular in 6 (30%). A foreign body giant cell reaction to the microspheres was uncommon (3 cases, 15%). We additionally performed a retrospective review of all gastrointestinal tissue obtained postprocedure from 784 sequential patients treated with Y90 microspheres. Three patients (0.4%) demonstrated the presence of resin microspheres upon histologic examination. No cases involving glass-based Y90 were identified (P=0.0078), despite the majority of patients having received glass radioembolization (630, 80%). This increased risk of secondary sphere dissemination is likely related to the increased number of particles required per activity for resin versus glass microspheres. We conclude that Y90 microspheres may be encountered in the gastrointestinal tract years after initial liver-targeted therapy and, when present, are often associated with mucosal ulceration. This finding is less likely to be encountered in patients who received Y90 radioembolization utilizing glass microspheres.
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