Hepatic basidiobolomycosis in a 2-year-old child: A case report

IF 0.2 Q4 PEDIATRICS
Ahmed Ateik , Saif Ghabisha , Ali Almutamaiz , Amar Almutawakel , Azza Mohamed , Faisal Ahmed
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引用次数: 0

Abstract

Introduction

Isolated hepatic basidiobolomycosis is infrequently reported in the literature. Hepatic involvement is typically associated with disseminated disease. Hepatic basidiobolomycosis can mimic hepatic malignancies, posing a diagnostic and therapeutic challenge.

Case presentation

A 2-year-old male was referred to us with a two-month history of abdominal pain and a right upper quadrant abdominal mass. He had no history of vomiting, jaundice, decreased appetite, or diarrhea. Laboratory tests showed leukocytosis (white blood cell count of 15.5 × 10⁹/L) with normal eosinophil count, elevated C-reactive protein (CRP; 30 mg/L; normal: <3 mg/L) and elevated erythrocyte sedimentation rate (ESR; 83 mm/h; normal: <10 mm/h). Liver function tests were within normal limits. Abdominal ultrasonography (USG) showed a well-defined isoechoic homogenous 7 × 7 × 6 cm mass-like lesion in the right hepatic lobe. An abdominal computed tomography (CT) scan confirmed a localized irregular hypodense area in the right hepatic lobe, raising concerns for a hepatic abscess or malignancy. However, tumor markers were not able to be measured. A true-cut needle biopsy showed primarily normal liver tissue with eosinophilic infiltration, proving inconclusive. Fungal cultures were unavailable. The patient was taken to the operating room for an exploration. We find a non-encapsulated mass in the right hepatic lobe, without any other gastrointestinal involvement. Intraoperative biopsies were not available, so we decided to proceed with a complete resection of the mass. The histopathological analysis showed Splendore-Hoeppli bodies and eosinophils around thin-walled hyphae, strongly supporting the diagnosis of basidiobolomycosis. The patient recovered well from the operation and received voriconazole (6 mg/kg every 12 hours) for six months. At two years of follow-up, he has no signs of recurrence.

Conclusion

Hepatic basidiobolomycosis should be included in the differential diagnosis of children with a painful hepatic mass. The lack of proper diagnosis can lead to unnecessary liver resections.
2岁儿童肝担子孢子菌病1例报告
文献中很少报道孤立性肝担子黑菌病。肝脏受累通常与播散性疾病有关。肝担子黑菌病可以模拟肝脏恶性肿瘤,提出了诊断和治疗的挑战。病例介绍一名2岁男童,因腹痛及右上腹肿块两个月来就诊。患者无呕吐、黄疸、食欲减退或腹泻史。实验室检查显示白细胞增多(白细胞计数15.5 × 10⁹/L),嗜酸性粒细胞计数正常,c反应蛋白(CRP)升高;30毫克/升;正常:3mg /L)和红细胞沉降率升高(ESR;83毫米/小时;正常:10mm /h)。肝功能检查在正常范围内腹部超声(USG)示右肝叶一清晰等回声均匀7 × 7 × 6 cm肿块样病灶。腹部计算机断层扫描(CT)证实在右肝叶局部不规则低密度区,引起肝脓肿或恶性肿瘤的关注。然而,肿瘤标志物无法测量。真切穿刺活检主要显示正常肝组织伴嗜酸性粒细胞浸润,结果不确定。无法进行真菌培养。病人被带到手术室进行检查。我们在右肝叶发现一个未包裹的肿块,没有其他胃肠道受累。术中没有活检,所以我们决定对肿块进行完全切除。组织病理学分析显示薄壁菌丝周围有splendohoeppli小体和嗜酸性粒细胞,有力支持担子黑菌病的诊断。患者术后恢复良好,连续6个月给予伏立康唑(6 mg/kg / 12小时)治疗。在两年的随访中,他没有复发的迹象。结论肝担子孢子菌病应列入儿童肝痛性肿块的鉴别诊断。缺乏正确的诊断会导致不必要的肝脏切除。
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
CiteScore
0.60
自引率
25.00%
发文量
348
审稿时长
15 days
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