Kuzman Ilija, Kirac Petar, Kuzman Tomislav, Puljiz Ivan, Bilić Vide
Klinika za infektivne bolesti Dr. Fran Mihaljević Zagreb, Hrvatska.
Acta Med Croatica. 2003;57(2):141-3.
Spontaneous splenic rupture is a rare but potentially fatal complication of infectious mononucleosis. Abdominal pain is uncommon in infectious mononucleosis, and splenic rupture should be strongly considered whenever abdominal pain occurs. The onset of pain may be insidious or abrupt. The pain is usually in the left upper quadrant.
To indicate that infectious mononucleosis is not always the innocent kissing disease, but could be complicated with splenic rupture as a life-threathenig condition.
CASE-REPORT: Our first case is described and a short literature review is provided. We report on the case of a 27-year-old man with infectious mononucleosis who had spontaneous splenic rupture that was successfully managed by splenectomy. On admission, he was febrile (38.5 degrees C) with hepatosplenomegaly, and had a blood pressure of 100/70 mm Hg. Six hours later, the patient complained of increasing abdominal pain. Abdominal ultrasound and computed tomography showed a 16.5 cm heterogeneous splenomegaly with subcapsular hematoma as well as free ascites. Laparotomy confirmed spontaneous rupture of the splenic capsule with active abdominal bleeding. Splenectomy was performed with a good clinical response. Examination of the spleen revealed a ruptured capsule with a subcapsular hematoma.
Infectious mononucleosis is the most common infectious disease to result in spontaneous spleen rupture. The prognosis is favorable when diagnosis is made on time and correct treatment is started immediately. Although splenectomy was advocated as definitive therapy in the past, numerous recent reports have documented good outcomes with non-operative management. Based on the literature review, an approach to the management of a spontaneously ruptured spleen secondary to infectious mononucleosis is suggested. Non-operative management can be successful in hemodynamically stable patients, i.e. in patients with subcapsular hematoma without overt rupture of the capsule to avoid complications of splenectomy (e.g. post-splenectomy sepsis).
We report on a 27-year-old man with infectious mononucleosis who had spontaneous splenic rupture that was successfully managed by splenectomy.
自发性脾破裂是传染性单核细胞增多症一种罕见但可能致命的并发症。腹痛在传染性单核细胞增多症中并不常见,每当出现腹痛时都应高度怀疑脾破裂。疼痛发作可能隐匿或突然。疼痛通常位于左上腹。
表明传染性单核细胞增多症并非总是无害的“亲吻病”,而是可能并发脾破裂这一危及生命的状况。
描述了我们的首例病例并进行了简短的文献综述。我们报告了一名27岁患有传染性单核细胞增多症的男性病例,其发生自发性脾破裂,通过脾切除术成功治疗。入院时,他发热(38.5摄氏度),伴有肝脾肿大,血压为100/70毫米汞柱。6小时后,患者主诉腹痛加剧。腹部超声和计算机断层扫描显示脾脏肿大16.5厘米,有包膜下血肿以及游离腹水。剖腹手术证实脾包膜自发性破裂并有腹腔内活动性出血。行脾切除术后临床反应良好。脾脏检查显示包膜破裂并有包膜下血肿。
传染性单核细胞增多症是导致自发性脾破裂最常见的传染病。若能及时诊断并立即开始正确治疗,预后良好。尽管过去主张脾切除术作为确定性治疗方法,但近期众多报告记录了非手术治疗的良好效果。基于文献综述,提出了一种针对传染性单核细胞增多症继发自发性脾破裂的处理方法。非手术治疗对于血流动力学稳定的患者可能成功,即对于有包膜下血肿但包膜未明显破裂的患者,可避免脾切除术后的并发症(如脾切除术后败血症)。
我们报告了一名27岁患有传染性单核细胞增多症的男性病例,其发生自发性脾破裂,通过脾切除术成功治疗。