Surgical neurology international · 2026
BurstDR spinal cord stimulation for chronic regional pain syndrome secondary to Castleman's disease treatment: A case report.
Клинический случайСтатьяНазвание и аннотация: Перевод пока не подготовлен
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.
Jaffee Stephen, Onyiah Chinelo, Patterson Michael D, White Griffin, Porwal Mokshal H, Tomycz Nestor
Аннотация
BACKGROUND: Castleman's disease is a rare lymphoproliferative disorder that can affect lymph nodes anywhere in the body. Removal of the enlarged lymph nodes may lead to secondary nerve damage, potentially resulting in patients developing complex regional pain syndrome (CRPS) type 2. Spinal cord stimulation (SCS) is a well-established, cost-effective therapy for chronic refractory pain, including CRPS type 2.
CASE DESCRIPTION: A 32-year-old female who was treated for unicentric hyaline vascular type Castleman's disease. Following neurolysis, she developed CRPS type 2 of the lumbosacral plexus; her symptoms persisted despite pharmacotherapy and physical therapy. She underwent a trial of burst SCS with significant symptom relief, followed by permanent implantation of a Penta paddle lead at the T8 level. Three months postoperatively, she reported marked clinical improvement and was able to discontinue pregabalin.
CONCLUSION: A 32-year-old female with Castleman's disease developed CRPS type 2 secondary to neurolysis that was effectively treated with Burst SCS.
CASE DESCRIPTION: A 32-year-old female who was treated for unicentric hyaline vascular type Castleman's disease. Following neurolysis, she developed CRPS type 2 of the lumbosacral plexus; her symptoms persisted despite pharmacotherapy and physical therapy. She underwent a trial of burst SCS with significant symptom relief, followed by permanent implantation of a Penta paddle lead at the T8 level. Three months postoperatively, she reported marked clinical improvement and was able to discontinue pregabalin.
CONCLUSION: A 32-year-old female with Castleman's disease developed CRPS type 2 secondary to neurolysis that was effectively treated with Burst SCS.