Tradisi pernikahan mabang handak disuku kayuagung ogan komering ilir (OKI) Tujuan penelitian ini untuk mengetahui prosesperkawinan pada masyarakat adat morge siwe di Kayuangung Kabupaten Ogan Komering Ilir. Metode yang digunakan dalam ialah metode deskriptif dengan teknik pengumpulan data adalah observasi dan wawancara. Hasil didapat oleh peneliti yaitu perkawinan merupakan proses sangat lengka...

Histiocytosis is a heterogenous group of disorders that are characterized by proliferation and activation of mononuclear phagocyte system. Langerhans Cell Histiocytosis (LCH) or Class I histiocytosis is a rare disorder of unknown etiology with proliferation of Langerhan cells which may infiltrate a single or multiple organs. This disease is more common in infants and children. It is usually spo...

Of 76 children with histiocytosis X 18 had orbital involvement, and four developed additional neuro-ophthalmic complications. No instance of intraocular involvement was detected. Among those patients with ophthalmic involvement the main problems were bilateral or unilateral proptosis, ptosis, papilloedema, optic atrophy, and seventh nerve palsy. Only one patient developed a severe visual defect...

Langerhans cell histiocytosis (LCH) is a rare disease, of unknown pathogenesis, characterized by intense and abnormal proliferation of bone marrow-derived histiocytes (Langerhans cells). It can present both local and systemic manifestations involving bone, skin and mucosal tissue, and internal organs. Three basic clinical forms develop: Letterer-Siwe disease (subacute or acute disseminated form...

During the last few years increasing attention has been focused on Langerhans cells and their peculiar granules (1-5). These organelles were considered specific products of the intraepidermal dendritic cells (1-3), but recently identical structures have been observed in osseous and pulmonary lesions of histiocytosis X (6). The Langerhans cell granule resembles a tennis racket. It is rodlike wit...

A four-year-old male child presented with increased Typically the lesions are round or oval-shaped with wellurine output and excessive thirst for eight months. On defined margins and bevelled edge. Individual lesions examination he had multiple scalp swellings with mild may coalesce giving a geographic appearance to the skull hepatosplenomegaly. Urine specific gravity was decreased suggestive o...

Langerhans cell histiocytosis (LCH), formerly known as histiocytosis X, refers to a spectrum of diseases characterized by idiopathic proliferation of histiocytes that produce either focal (localized LCH) or systemic manifestations (Hand-Schüller-Christian disease and Letterer-Siwe disease). Localized LCH accounts for approximately 60-70 % of all LCH cases. Osseous involvement is the most common...

BACKGROUND Congenital self-healing Langerhans cell histiocytosis (Hashimoto-Pritzker disease) is the rarest form of Langerhans cell histiocytosis, usually confined to the skin and/or mucous membranes. Cutaneous eruption is mostly generalized, papular, nodular or vesicular. Despite impressive clinical presentation in a newborn it infrequently spreads to internal organs (which then portends a gra...