A Case of a Huge Iliopsoas Abscess that Perforated and Communicated with the Ureter.

IF 1.5 Q2 MEDICINE, GENERAL & INTERNAL JMA journal Pub Date : 2024-07-16 Epub Date: 2024-06-03 DOI:10.31662/jmaj.2023-0217
Yusuke Tabata, Masato Yanagi, Kazuo Enomoto, Satoshi Omori, Noriyoshi Murotani, Osamu Mitsuhashi, Mitsunori Yasuda, Yuki Sawano, Koichiro Omori, Yoichiro Tabata, Tokifumi Majima
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Abstract

We experienced a rare case in which iliopsoas abscess (IPA), caused by an Extended Spectrum β-Lactamase (ESBL)-producing Proteus mirabilis, perforated and communicated with the ureter and caused sepsis. An 84-year-old woman, bedridden due to sequelae of a cerebral hemorrhage, was brought to our hospital with a chief complaint of fever lasting for 3 weeks. Computed tomography (CT) revealed a huge 180 × 110 × 100 mm IPA in the right iliopsoas muscle. The ureter was also found to communicate with the iliopsoas muscle abscess, ureteral stenosis was detected at the same site, and dilatation of the renal pelvis occurred above the area of the ureteral stenosis, indicating hydronephrosis. Considering the mechanism of this case, if the ureter first ruptures and urine leaks, followed by the formation of an IPA, urine will flow along the surrounding fatty tissue and cause an abscess around the ureter and kidney. However, because almost no abscess was detected around the ureter, the abscess was thought to have originated from the iliopsoas muscle located near the center of the ureter. In summary, in this case, an abscess first formed within the iliopsoas muscle, which gradually expanded and compressed the right ureter, resulting in hydronephrosis. The upper ureter, which had become dilated and thinned due to ureteral obstruction, became even more fragile because of the spread of inflammation from the IPA, and the IPA perforated and communicated with the ureter. In patients who have difficulty communicating, the diagnosis of IPA may be delayed because the only symptom is fever. As in this case, if the diagnosis is delayed, the abscess may become large and perforate the ureter; thus, IPA should always be considered as a cause of fever of unknown origin.

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一例巨大髂腰肌脓肿穿孔并与输尿管相通的病例
我们曾经历过一例罕见病例,由产广谱β-内酰胺酶(ESBL)的奇异变形杆菌引起的髂腰肌脓肿(IPA)穿孔并与输尿管相通,导致败血症。一名 84 岁的妇女因脑出血后遗症卧床不起,以持续 3 周的发热为主诉被送到我院。计算机断层扫描(CT)显示,右侧髂腰肌有一个 180 × 110 × 100 毫米的巨大 IPA。还发现输尿管与髂腰肌脓肿相通,同一部位发现输尿管狭窄,输尿管狭窄区域上方出现肾盂扩张,表明存在肾积水。考虑到该病例的发病机制,如果输尿管首先破裂导致尿液漏出,然后形成 IPA,尿液就会沿着周围的脂肪组织流动,导致输尿管和肾脏周围出现脓肿。然而,由于输尿管周围几乎未发现脓肿,因此认为脓肿源于输尿管中心附近的髂腰肌。总之,在该病例中,脓肿首先在髂腰肌内形成,然后逐渐扩大并压迫右侧输尿管,导致肾积水。因输尿管梗阻而扩张变细的输尿管上段,由于 IPA 炎症的扩散而变得更加脆弱,IPA 穿孔并与输尿管相通。对于交流困难的患者,IPA 的诊断可能会因为其唯一的症状是发烧而被延误。就像本病例一样,如果延误诊断,脓肿可能变大并穿破输尿管;因此,IPA 应始终被视为不明原因发热的病因。
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