Teja K, Sabio H, Langdon D R, Johanson A J
Hum Pathol. 1981 Dec;12(12):1137-9. doi: 10.1016/s0046-8177(81)80334-6.
A 27 month old white male infant clinically suspected of having histiocytosis X had an enlarged hard hypofunctioning thyroid. A needle biopsy of the thyroid showed disruption of the thyroid architecture by an infiltrate consisting of large histiocytes admixed with eosinophils, neutrophils, and lymphocytes, confirming the clinical diagnosis of histiocytosis X.
一名27个月大的白人男婴临床上疑似患有朗格汉斯细胞组织细胞增生症,其甲状腺肿大且功能减退。甲状腺穿刺活检显示,由大组织细胞与嗜酸性粒细胞、中性粒细胞和淋巴细胞混合组成的浸润物破坏了甲状腺结构,从而证实了朗格汉斯细胞组织细胞增生症的临床诊断。