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一位 28 岁女性,因系统性红斑狼疮临床发作和腹痛就诊,病因是腹直肌鞘血肿。

A 28-Year-Old Woman Presenting with a Clinical Flare of Systematic Lupus Erythematosus and Abdominal Pain Due to Rectus Sheath Hematoma.

机构信息

Department of Nephrology, Peking University Shenzhen Hospital, Shenzhen, Guangdong, China (mainland).

The George Institute for Global Health and University of New South Wales, Newtown, NSW, Australia.

出版信息

Am J Case Rep. 2022 Jun 15;23:e935472. doi: 10.12659/AJCR.935472.

Abstract

BACKGROUND A flare, or flare-up, of systematic lupus erythematosus (SLE) is diagnosed by an increase in disease activity in one or more organs, new symptoms, or changes in laboratory measurements. A hematoma can occur in the sheath of the rectus abdominis following muscle trauma or rupture of an epigastric vessel, or it can occur spontaneously. This report is of a 28-year-old woman who presented with a clinical flare of SLE and abdominal pain due to rectus sheath hematoma. CASE REPORT A 28-year-old woman had been suspected of having SLE 9 years ago and had received glucocorticoid therapy combined with hydroxychloroquine. However, lupus flared after she discontinued glucocorticoids, and she was admitted with a 1-month history of marked generalized edema, abdominal distension, frothy urine, and massive ascites. During hospitalization, she abruptly developed a continuous, stabbing abdominal pain and a bulge over the right abdomen as a result of straining during a bowel movement. On examination, a well-demarcated round mass that measured 121 mm × 96 mm was detected in the right quadrant. Abdominal emergency computed tomography revealed a right rectus sheath hematoma (21.4×4.7 cm). After her condition improved, the patient underwent an ultrasound-guided renal biopsy and was diagnosed with class III (A/C) and class V lupus nephritis. CONCLUSIONS This case has shown that spontaneous rectus sheath hematoma can occur without a history of trauma in a patient with an exacerbation of SLE. This association appears to be rare, and the cause is unknown.

摘要

背景

系统性红斑狼疮 (SLE) 发作或加剧是通过一个或多个器官的疾病活动增加、新症状或实验室测量值的变化来诊断的。血肿可在腹直肌鞘中发生,原因是肌肉创伤或上腹部血管破裂,也可自发发生。本报告介绍了一位 28 岁女性,她因 SLE 临床发作和腹直肌鞘血肿引起的腹痛就诊。

病例报告

一位 28 岁女性 9 年前被怀疑患有 SLE,并接受了糖皮质激素联合羟氯喹治疗。然而,在她停用糖皮质激素后狼疮发作,因 1 个月来全身显著水肿、腹胀、泡沫尿和大量腹水而入院。住院期间,她因排便时用力突然出现持续性刺痛性腹痛和右腹部膨出。体格检查发现右上象限有一个边界清楚的圆形肿块,大小为 121mm×96mm。腹部急诊 CT 显示右侧腹直肌鞘血肿(21.4×4.7cm)。病情改善后,患者接受了超声引导下的肾活检,诊断为 III 级(A/C)和 V 级狼疮肾炎。

结论

本病例表明,在 SLE 加重的患者中,即使没有创伤史,也可能发生自发性腹直肌鞘血肿。这种关联似乎很少见,原因不明。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15d8/9208341/9dbb30a00b0f/amjcaserep-23-e935472-g001.jpg

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