Aricò M, Egeler R M
Department of Pediatrics, University of Pavia, IRCCS Policlinico San Matteo, Italy.
Hematol Oncol Clin North Am. 1998 Apr;12(2):247-58. doi: 10.1016/s0889-8588(05)70508-6.
Langerhans cell histiocytosis remains an enigmatic disease with protean manifestations. It may be self-limited in some, whereas in others, even intensive treatment is unsuccessful. The outcome depends on whether vital organ function is compromised at diagnosis or shortly thereafter, in which case the prognosis is grave.
朗格汉斯细胞组织细胞增多症仍然是一种具有多样临床表现的神秘疾病。它在一些患者中可能是自限性的，而在另一些患者中，即使进行强化治疗也不成功。其预后取决于在诊断时或此后不久重要器官功能是否受到损害，在这种情况下预后很差。
