Searchable abstracts of presentations at key conferences in endocrinology
Endocrine Abstracts (2016) 41 EP299 | DOI: 10.1530/endoabs.41.EP299

ECE2016 Eposter Presentations Clinical case reports - Pituitary/Adrenal (81 abstracts)

Initial presentation with diabetes insipidus in langerhans cell histiocytosis, can be marker of multisystemic and progressive involvement

Nizameddin Koca 1 , Gamze Emlek 1 , Pinar Sisman 2 , Tuba Gullu Koca 3 , Ozlem Sengoren Dikis 5 , Ozen Oz Gul 2 & Soner Cander 4


1Bursa Yuksek Ihtisas Training and Research Hospital, Internal Medicine, Bursa, Turkey; 2Uludag University Medical School, Endocrinology and Metabolism, Bursa, Turkey; 3Bursa AOS Oncology Hospital, Internal Medicine, Bursa, Turkey; 4Bursa Yuksek Ihtisas Training and Research Hospital, Endocrinology and Metabolism, Bursa, Turkey; 5Bursa Yuksek Ihtisas Training and Research Hospital, Pulmonology, Bursa, Turkey.


Langerhans cell histiocytosis (LCH) is a rare histiocytic disorder most commonly characterized by osteolytic bone lesions. Central nervous system (CNS) involvement observed at 6% and Diabetes insipidus (DI) one of the important signs of CNS involvement.

A 40-years-old woman presented with polyuria, polydipsia and headache. Water deprivation test was compatible with DI. Magnetic resonance imaging (MRI) shows 4×4 mm focal thickening at the distal infundibular stalk. She was followed-up under desmopressin. At the sixth months of therapy, clinical situation negatively progressed with complaints of lethargy, diplopia, menstrual irregularity, headache and forgetfulness. MRI revealed progression of nodular thickness (18×15 mm) through hypothalamus. Secondary hypogonadism was detected while other pituitary functions were normal. Multiple, irregularly shaped cystic lesions at he posterior and upper lobes of lungs and multiple lymph nodes with max 20 mm diameter was observed in computed tomography. There were no bone lesion in direct radiographies and there was no skin involvement. Open thoracoscopic biopsy performed by surgeon and revealed LCH on histopathological examination with positive CD68, S100 and CD1a staining. After diagnosis, PET-scan performed and reveals increased osteoblastic activity at the 6th, 8th and 9th right ribs and in the central part of the left femoral shaft. Bone marrow biopsy was reported as normocellular. External radiotherapy and six cycle of chemotherapy (vinblastine+prednisolon) was planned. Also she was on desmopressin, prednisolone and levothyroxine treatment.

We reported this case to refer to diabetes insipidus as a rare presentation of Langerhans cell histiocytosis which a rare and some times multysystemic progressive disease. Diabetes insipidus, is an important indicator for stalk lesions and may be marker of very rare conditions such as atypical tumor of the sellar region, sarcoidosis, lymphocytic hypophysitis or histiocytosis like in this case. It should be monitored dynamically because of the possibility of progressive nature of the disease.

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