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镰状细胞病伴急性卒中的9岁女孩的毛糙骨征

Hair-on-End Sign in a 9-Year-Old Girl Presenting with Acute Stroke in Sickle Cell Disease.

作者信息

Ogwang Eugene, Odongo Charles Newton, Namusisi Jane, Okello Patrick Ambrose, Acan Moses

机构信息

Department of Radiology, Mbarara University of Science and Technology, Mbarara City, South-Western Uganda, Uganda.

Department of Surgery, Mbarara University of Science and Technology, Mbarara City, South-Western Uganda, Uganda.

出版信息

Int Med Case Rep J. 2022 Feb 24;15:69-73. doi: 10.2147/IMCRJ.S345847. eCollection 2022.

Abstract

BACKGROUND

The hair-on-end (HOE) sign is a rare finding seen in the diploic space on skull radiographs, computed tomography (CT) and magnetic resonance imaging (MRI) with the appearance of long, thin vertical striations of calcified spicules perpendicular to the bone surface that looks like hair standing on end. It is classically seen in children/adolescents with hemolytic anemias, in particular, thalassemia major and sickle cell disease. Here, we present a 9-year-old Ugandan girl who presented with stroke in whom head CT demonstrated cerebral intraparenchymal hemorrhage and multiple infarcts on the left with HOE sign. Hb electrophoresis confirmed the diagnosis of sickle cell anemia.

CASE SUMMARY

We present a 9-year-old Ugandan girl who presented with an unexplained stroke that preceded an episode of acute headache, vomiting, followed by focal convulsions and altered consciousness. Clinical findings revealed severe pallor of the conjunctivae and mild scleral icterus. CT demonstrated right cerebral intraparenchymal hemorrhage, multiple high cerebral infarcts on the right and evidence of extra medullary hematopoiesis with a classical HOE sign. Hemoglobin (Hb) electrophoresis confirmed sickle cell disease (SCD). The child was then initiated on hydroxyurea, antibiotics, analgesics and intravenous fluids. She improved and was discharged 16 days later. Follow-up of the child was uneventful.

CONCLUSION

HOE sign is a complication of chronic hemolysis usually seen in patients with thalassemia and sickle cell anemia. It is a rare finding that clinicians should be well conversant with, especially in Africa where sickle cell disease is common.

摘要

背景

梳状征(HOE)是在颅骨X线平片、计算机断层扫描(CT)和磁共振成像(MRI)的板障间隙中罕见的表现,呈现为垂直于骨表面的细长钙化针状垂直条纹,看起来像头发竖起。经典地见于患有溶血性贫血的儿童/青少年,特别是重型地中海贫血和镰状细胞病。在此,我们报告一名9岁的乌干达女孩,她因中风就诊,头部CT显示脑实质内出血和左侧多发梗死灶伴梳状征。血红蛋白电泳确诊为镰状细胞贫血。

病例摘要

我们报告一名9岁的乌干达女孩,她在出现急性头痛、呕吐,随后出现局灶性惊厥和意识改变之前发生了不明原因的中风。临床检查发现结膜严重苍白和轻度巩膜黄疸。CT显示右侧脑实质内出血、右侧多发高脑梗死灶以及髓外造血证据伴典型的梳状征。血红蛋白(Hb)电泳确诊为镰状细胞病(SCD)。然后该患儿开始使用羟基脲、抗生素、镇痛药和静脉输液治疗。她病情好转,16天后出院。对该患儿的随访情况良好。

结论

梳状征是慢性溶血的一种并发症,通常见于地中海贫血和镰状细胞贫血患者。这是一种罕见的表现,临床医生应熟知,尤其是在镰状细胞病常见的非洲地区。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf73/8885120/c4a51d84aa4d/IMCRJ-15-69-g0001.jpg

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