Gamby T, Pizzi M, Lebreuil G, Devaux J, Privat Y
Sem Hop. 1981;57(33-36):1402-8.
A typical case of Montgomery xanthomatosis is reported by the authors. Out of this case and of a hundred other ones gathered from the literature, they outline the main features of the disease. It is revealed as being stereotyped and particularly the prognosis is usually good. Whether the ultra structural study may show Langerhans corpuscules or not, it brings us a material to the discussing of border-line cases (xanthomatosis with diabetes insipidus, Hand-Schüller-Christian disease with cutaneous lesions similar to Montgomery's.
作者报告了一例典型的蒙哥马利黄瘤病病例。基于该病例以及从文献中收集的其他一百个病例，他们概述了该病的主要特征。该病表现为具有固定模式，尤其是预后通常良好。无论超微结构研究是否能显示朗格汉斯细胞，它都为我们讨论临界病例（伴有尿崩症的黄瘤病、伴有类似于蒙哥马利病皮肤损害的汉-许-克病）提供了素材。
