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传染性单核细胞增多症导致脾脏梗死的神秘病例:一种罕见情况。

A Mysterious Case of an Infarcted Spleen due to Kissing Disease: A Rare Entity.

作者信息

Pervez Hira, Tameez Ud Din Asim, Khan Ahmad

机构信息

Internal Medicine/Cardiology, Dow University of Health Sciences, Karachi, PAK.

Internal Medicine, Rawalpindi Medical University, Rawalpindi, PAK.

出版信息

Cureus. 2020 Jan 19;12(1):e6700. doi: 10.7759/cureus.6700.

Abstract

Viruses are long known to be leading causes of self-limiting infections. Infectious mononucleosis (IM) caused by the Epstein-Barr virus (EBV) is, however, no exception. The ailment is caused by a DNA virus belonging to the Herpesviridae family. As stated earlier, the infection is usually self-limited with mononucleosis-like symptoms such as fever, sore throat, lymphadenopathy (LAD), rash, headache, etc. In rare instances, it can lead to severe complications. The organ of prime importance following the infection is spleen. There are occasions where splenic injuries can lead to rupture, deeming to emergency surgical interventions. At other times, a rare entity may also be seen that constitutes an infarction within the splenic substance. We present this rare finding in a 20-year-old male patient with a left upper quadrant (LUQ) pain, cervical LAD, and sore throat who was brought to the emergency department. On physical examination, mild tenderness was observed in the LUQ with an inflamed throat and palpable cervical and occipital lymph nodes. Laboratory investigations suggested lymphocytosis with no blast cells, lactic acidosis, and mild acute kidney injury. A contrast-enhanced computed tomography scan demonstrated an enlarged spleen with wedge-shaped hypodense areas, which led to a diagnosis of splenic infarction secondary to infectious mononucleosis. Keeping in mind the symptomatology and the age of the patient, a bunch of differentials were needed to be ruled out. Out of a series of investigations done on the patient, EBV serology for IgM was positive. The patient was conservatively treated with a complete resolution of symptoms in one month. Our case adds to the literature the finding of a rare etiology of splenic infarction secondary to IM and the importance of stepwise and cost-effective investigations to avoid unnecessary workup when needed.

摘要

长期以来,病毒一直被认为是自限性感染的主要原因。然而,由爱泼斯坦-巴尔病毒(EBV)引起的传染性单核细胞增多症(IM)也不例外。这种疾病是由一种属于疱疹病毒科的DNA病毒引起的。如前所述,该感染通常是自限性的,伴有单核细胞增多症样症状,如发热、喉咙痛、淋巴结病(LAD)、皮疹、头痛等。在极少数情况下,它会导致严重并发症。感染后最重要的器官是脾脏。有时脾损伤会导致破裂,需要紧急手术干预。其他时候,还可能会出现一种罕见的情况,即脾脏实质内出现梗死。我们在此报告一名20岁男性患者的这一罕见发现,该患者因左上腹(LUQ)疼痛、颈部淋巴结肿大和喉咙痛被送往急诊科。体格检查发现左上腹有轻度压痛,喉咙发炎,颈部和枕部淋巴结可触及。实验室检查提示淋巴细胞增多,无原始细胞,乳酸酸中毒,轻度急性肾损伤。增强计算机断层扫描显示脾脏肿大,有楔形低密度区,诊断为传染性单核细胞增多症继发脾梗死。考虑到患者的症状和年龄,需要排除一系列不同的疾病。在对该患者进行的一系列检查中,IgM的EBV血清学检查呈阳性。患者接受了保守治疗,一个月后症状完全缓解。我们的病例为文献增添了传染性单核细胞增多症继发脾梗死这一罕见病因的发现,以及逐步进行且具有成本效益的检查的重要性,以避免在必要时进行不必要的检查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/766a/7029827/82e11b4bd13b/cureus-0012-00000006700-i01.jpg

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