Histiocytose langerhansienne multiviscérale associée à un syndrome d'interruption de la tige pituitaire

Conclusion. - Although, some events of his perinatal history lead to the hypothesis of a malformative origin, the progression of Langerhans'cell histiocytosis affected tissues to fibrosis, suggest that this disease is the cause of the patient's hypothalamohypophyseal lesions.