𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Pulmonary and mediastinal lesions in children with Langerhans cell histiocytosis

✍ Scribed by Anne Smets; Koen Mortelé; Gunther De Praeter; Olivier François; Yves Benoit; Marc Kunnen

Publisher
Springer-Verlag
Year
1997
Tongue
English
Weight
147 KB
Volume
27
Category
Article
ISSN
0301-0449

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Neuropsychologic deficits in children wi
Neuropsychologic deficits in children with Langerhans cell histiocytosis
✍ Whitsett, Stan F.; Kneppers, Kirstie; Coppes, Max J.; Egeler, R. Maarten 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 164 KB 👁 2 views

Background. Manifestations of Langerhans cell histiocytosis (LCH) in children range from only a rash, to bony lesions accompanied by pain, to major organ disease. When the central nervous system (CNS) is affected, the LCH patient may exhibit signs and symptoms of hypothalamic and pituitary dysfuncti

Radiation therapy in soft-tissue lesions
Radiation therapy in soft-tissue lesions in histiocytosis X (Langerhans' cell histiocytosis)
✍ Gramatovici, Razvan ;D'Angio, Giulio J. 📂 Article 📅 1988 🏛 John Wiley and Sons 🌐 English ⚖ 341 KB

Langerhans' cell histiocytosis (LCH) (previously histiocytosis X) is an infrequent disease with protean clinical manifestations and an unpredictable course. The role of radiotherapy in the soft tissue complications of LCH was evaluated in this retrospective study of 40 patients seen in two major Phi

Etoposide in the treatment of six childr
Etoposide in the treatment of six children with langerhans cell histiocytosis (histiocytosis X)
✍ Viana, Marcos Borato ;Oliveira, Benigna Maria ;Silva, Celia Maria ;Leite, Virgin 📂 Article 📅 1991 🏛 John Wiley and Sons 🌐 English ⚖ 548 KB

Six children received etoposide as the single agent for treatment of Langerhans cell histiocytosis (LCH; histiocytosis X). Five were less than 2 years old at diagnosis. All had multiorgan involvement; one had liver and pulmonary dysfunction. Two infants also had clinical signs of immune deficiency.

Langerhans' cell histiocytosis: Head and
Langerhans' cell histiocytosis: Head and neck manifestations in children
✍ Mr. Muhammad S. Quraishi; Mr. Alexander W. Blayney; Mr. David Walker; Mr. Fin B. 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 English ⚖ 596 KB

Background. Langerhans' cell histiocytosis (LCH) is an uncommon, poorly understood granulomatous disease, characterized by the idiopathic proliferation of Langerhan's cells or their marrow precursors. In 1985, the Philadelphia Workshop adopted the term "Langerhans' cell histiocytosis" (LCH) to diffe