Spontaneous splenic rupture as the first manifestation of chronic myeloid leukemia: A case report.

Q3 Medicine
Qatar Medical Journal Pub Date : 2026-06-23 eCollection Date: 2026-01-01 DOI:10.5339/qmj.2026.47
Albaraa Rustom, Zeinab Ibrahim, Yaman Alahmad, Omar Jamil, Rayan Mahgoub, Salman Mirza
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引用次数: 0

Abstract

Background: Spontaneous splenic rupture (SSR) is an uncommon life-threatening complication of chronic myeloid leukemia (CML); however, it rarely occurs as the initial presentation of the disease. A contrast-enhanced computed tomography (CT) scan is the preferred method for confirming the diagnosis. The definitive treatment is radical splenectomy.

Case presentation: We report the case of a 37-year-old previously healthy man who presented to the Emergency Department with severe, vague abdominal pain and nausea of one day's duration. On physical examination, he had epigastric tenderness and palpable splenomegaly, while his vital signs were within the normal limits. Contrast-enhanced CT revealed massive splenomegaly and splenic rupture with active bleeding. Subsequently, the patient became hemodynamically unstable and required an urgent total splenectomy. Molecular cytogenetic tests showed abnormalities consistent with CML. The patient's condition gradually improved, and he was discharged home on the 10th postoperative day.

Discussion: SSR typically occurs in patients with preexisting hematologic disorders or constitutional symptoms. This case is unique because the patient, who had no history of trauma, constitutional symptoms, or a known hematologic disorder, presented with massive splenomegaly and extremely elevated leukocytosis and was found to have undiagnosed CML. The patient's massive splenomegaly and abrupt splenic rupture highlight that SSR can occur even in the absence of classic B symptoms, posing significant diagnostic and management challenges. Timely multidisciplinary intervention is crucial, and thorough post-splenectomy care is essential.

Conclusion: SSR as the initial manifestation of CML is an uncommon and unexpected clinical presentation. This case demonstrates that extreme leukocytosis and massive splenomegaly can precipitate splenic rupture in the absence of prodromal symptoms. Timely surgical intervention, comprehensive post-splenectomy care, and the prompt initiation of targeted therapy are indispensable for achieving optimal clinical outcomes, as demonstrated in our patient.

自发性脾破裂为慢性髓性白血病的首发表现:1例报告。
背景:自发性脾破裂(SSR)是慢性髓性白血病(CML)中一种罕见的危及生命的并发症;然而,它很少作为疾病的初始表现出现。对比增强计算机断层扫描(CT)是确认诊断的首选方法。最终的治疗是根治性脾切除术。病例介绍:我们报告一个37岁以前健康的人谁提出了严重的,模糊的腹痛和恶心持续一天的急诊科的情况。体格检查发现上腹压痛,脾肿大可触及,生命体征正常。增强CT显示脾肿大及脾破裂伴活动性出血。随后,患者血流动力学不稳定,需要紧急全脾切除术。分子细胞遗传学检查显示异常与CML一致。患者病情逐渐好转,于术后第10天出院。讨论:SSR通常发生在既往存在血液疾病或体质症状的患者中。这个病例是独特的,因为病人没有外伤史,体质症状,或已知的血液系统疾病,表现为脾肿大和白细胞异常升高,被发现患有未确诊的CML。患者的巨大脾肿大和突然脾破裂表明,即使没有典型的B症状,SSR也可能发生,这给诊断和治疗带来了重大挑战。及时的多学科干预至关重要,彻底的脾切除术后护理是必不可少的。结论:SSR作为CML的首发表现是一种罕见的、出乎意料的临床表现。本病例表明,在没有前驱症状的情况下,极端的白细胞增多和巨大的脾肿大可导致脾破裂。及时的手术干预,全面的脾切除术后护理,及时开始靶向治疗是获得最佳临床结果所不可或缺的,正如我们的患者所证明的那样。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Qatar Medical Journal
Qatar Medical Journal Medicine-Medicine (all)
CiteScore
1.80
自引率
0.00%
发文量
77
审稿时长
6 weeks
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