Borda J M, Abulafia J, Valda L
Med Cutan Ibero Lat Am. 1977;5(1):21-31.
The Woringer-Kolopp's disease must be considered a clinical-pathologic variant of mycosis fungoides. It is characterized by heterogenous clinical features and a peculiar histological aspect given by the cellular infiltration of the epidermis. The orgin of the reticular elements is discussed. Though some investigators think they originate in the dermis, others consider their origin to be "in situ". The evolution and prognosis are not well defined, as is the case with the hyperplastic, heteromorphic and polymorphic reticuloses. The case presented has had Hodgkin's disease and then developed a picture of pagetoid reticulosis.
沃林格-科洛普病必须被视为蕈样肉芽肿的一种临床病理变体。它具有异质性的临床特征以及由表皮细胞浸润所呈现出的独特组织学表现。文中讨论了网状细胞成分的起源。尽管一些研究者认为它们起源于真皮，但另一些人则认为其起源是“原位”的。其演变和预后并不明确，增生性、异型性和多形性网状细胞增多症的情况也是如此。所呈现的病例曾患有霍奇金病，随后发展为派杰样网状细胞增多症的表现。
