Histiocytosis in Nigerian children: A report of two variants

E. Udo, I. Precious Oloyede, E. Bassey, O. Udoh
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Abstract

Histiocytoses are a rare group of proliferative disorders with very similar clinical and histological pictures. We present a case report of two variants seen in an eight-month-old female and five-month-old male in a tertiary hospital in southern Nigeria. They both presented with painless neck swellings and fever, leucocytosis, neutrophilia and lymphopenia. Initial histologic examinations of the cervical lymph nodes biopsy posed a diagnostic conundrum. However, Immuno-histochemical analysis done on both sample showed CD1a, positive S100 in keeping with Langerhans cell histiocytosis in the former. While, that of the latter showed strongly positive CD68, positive S-100 in 30% cells in keeping with Sinus histiocytosis with massive lymphadenopathy (SLMH) in the latter. Clinicians should have a high index of suspicion for histiocytosis in children presenting with generalised lymphadenopathy. Also, apart from the routine histology, immunohistochemistry analysis is recommended for all cases
尼日利亚儿童组织细胞增多症:两种变异的报告
组织细胞增多症是一种罕见的增殖性疾病,具有非常相似的临床和组织学表现。我们报告了尼日利亚南部一家三级医院一名8个月大的女婴和一名5个月大的男婴出现两种变异的病例报告。患者均表现为无痛性颈部肿胀、发热、白细胞增多、中性粒细胞增多和淋巴细胞减少。颈部淋巴结活检的初步组织学检查提出了一个诊断难题。然而,对两个样本进行的免疫组织化学分析显示CD1a, S100阳性,与前者的朗格汉斯细胞组织细胞增多症保持一致。而后者的CD68呈强阳性,S-100阳性的细胞占30%,与后者的窦性组织细胞增生伴大量淋巴结病(SLMH)一致。临床医生应该对全身性淋巴结病患儿的组织细胞增多症有高度的怀疑。此外,除常规组织学检查外,建议对所有病例进行免疫组织化学分析
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