Nasal oral fistula revealing Langerhans' cell histiocytosis in adult patient: case report
A. Mzabi, Maissa Thabet, Taghrid Tlili, Hend Zorgati, J. Anoun, Imen Ben Hassine, Monia Karmeni, Fatma Ben Fredj, Moncef Mokni, Chadia Laouani
Abstract
A. Mzabi, Maissa Thabet, Taghrid Tlili, Hend Zorgati, J. Anoun, Imen Ben Hassine, Monia Karmeni, Fatma Ben Fredj, Moncef Mokni, Chadia Laouani
Abstract
Langerhans cell histiocytosis (LCH) is a rare systemic disease caused by proliferation of mature histiocytes; its association to histiocyto fibroma is rarely reported. It rarely affects adults. We report a case of systemic LCH, in an adult patient with osteolytic lesion causing a fistula between the left nasal cavity and hard palate, involving the bone, lung, lymph node and associated to multiple histiocyto fibroma. The patient was operating for a fistula, and he was treated by chemotherapy and corticosteroids. Langerhans´ cell histiocytosis is a rare case, especially in adult patient. The diagnosis was based on histological and immunohistochemical analyses. This patient was treated by steroids and chemotherapy.
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Langerhans cell histiocytosis (LCH) is a rare systemic disease caused by proliferation of mature histiocytes; its association to histiocyto fibroma is rarely reported. It rarely affects adults. We report a case of systemic LCH, in an adult patient with osteolytic lesion causing a fistula between the left nasal cavity and hard palate, involving the bone, lung, lymph node and associated to multiple histiocyto fibroma. The patient was operating for a fistula, and he was treated by chemotherapy and corticosteroids. Langerhans´ cell histiocytosis is a rare case, especially in adult patient. The diagnosis was based on histological and immunohistochemical analyses. This patient was treated by steroids and chemotherapy.
Key concepts: Medicine, Langerhans cell histiocytosis, Histiocyte, Histiocytosis, Nasal cavity, Lesion, Pathology, Rare disease