Journal of orthopaedic case reports · 2025
A Missed Case of Langerhans Cell Histiocytosis of the Proximal Femur after Total Hip Arthroplasty in an Adult: A Case Report.
Клинический случайСтатьяНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Sehrawat Sandeep, Ojha Mukund Madhav, Gamanagatti Shivanand, Kumar Vijay
Аннотация
INTRODUCTION: Langerhans cell histiocytosis (LCH) is a rare disease primarily affecting children. The occurrence of osseous LCH is rare in adults. The lytic lesion of LCH can resemble the lytic lesion of septic or aseptic loosening in an operated case of arthroplasty.
CASE REPORT: We report an operated case of total hip arthroplasty whose peri-prosthetic lesion was uncertain by clinical and radiological investigations. Later, a core biopsy revealed the unexpected diagnosis of LCH.
CONCLUSION: LCH is an infrequent phenomenon in an adult. This experience taught us the importance of core biopsy and phenotyping in patients with doubtful cystic-lytic lesions over the bone adjacent to the prosthesis.
CASE REPORT: We report an operated case of total hip arthroplasty whose peri-prosthetic lesion was uncertain by clinical and radiological investigations. Later, a core biopsy revealed the unexpected diagnosis of LCH.
CONCLUSION: LCH is an infrequent phenomenon in an adult. This experience taught us the importance of core biopsy and phenotyping in patients with doubtful cystic-lytic lesions over the bone adjacent to the prosthesis.