A rare case of coexistence of pulmonary adenocarcinoma with Langerhans’ cell histiocytosis
✍ Scribed by Yuji Ohtsuki; Masashi Uomoto; Yasuki Hachisuka; Miyuki Kato; Mitsuko Iguchi; Gang-Hong Lee; Mutsuo Furihata
- Publisher
- Springer
- Year
- 2008
- Tongue
- English
- Weight
- 394 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0918-4287
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## Abstract ## Background In Langerhans cell histiocytosis (LCH) pulmonary involvement, which is often initially asymptomatic, may contribute to significant morbidity and mortality. To determine the long‐term prognosis, a cross‐sectional study was undertaken. ## Procedure Forty‐one patients with
We report a case of Langerhans' cell histiocytosis (LCH) occurring after a living donor liver transplantation (LDLT) for fulminant hepatitis. A 9-month-old girl underwent an LDLT for fulminant hepatitis of an unknown cause. The histology of the native liver did not show any findings of LCH. On posto