Spontaneous Regression Of Brown Tumor In A Patient Treated With Peritoneal Dialysis
Ito, K., Ikuta, K., Nishida, Y., Sakai, T., & Imagama, S. (2021). Spontaneous Regression of Brown Tumor in a Patient Treated With Peritoneal Dialysis. Cureus, 13(8), e17078. https://doi.org/10.7759/cureus.17078
View Original Source →Abstract
A 52-year-old man, with a history of diabetic nephropathy and renal cancer, had been treated with peritoneal dialysis for four months before consulting our hospital. At the time of imaging evaluation, three years after surgery for renal cancer, fluorodeoxyglucose accumulation was found at the distal metaphysis of the left radius. After the biopsy, he was diagnosed with giant cell tumor of bone (GCTB), and surgery was scheduled. However, osteogenesis was observed in the images retaken before surgery. It was found that his intact parathyroid hormone level had been abnormally high four months prior to his visit to us but had subsequently normalized. The tissue obtained by re-biopsy revealed osteogenesis with the disappearance of multinucleated giant cells, suggesting a brown tumor (BT). The tumor was thought to have been caused by secondary hyperparathyroidism (HPT) associated with peritoneal dialysis. When osteolytic lesions mimicking GCTB are found, the possibility of BT should be considered based on comorbidities and clinical information.
Case Details
Disease Location
Radius
Personal Characteristics
52-year-old man. History of ckd due to microvascular nephrotic syndrome and diabetic nephropathy. The patient had undergone a unilateral partial nephrectomy for renal cancer three years before.
Clinical Characteristics
Referred because of abnormal accumulation at the distal metaphysis of the left radius on an fdg-PET scan taken for follow-up after renal cancer. Laboratory data showed slightly low levels of various electrolytes in addition to renal dysfunction, consistent with the hemodialysis state. A geographic radiolucent lesion with sclerotic margins was found in the radiographs taken at the initial consultation. The tumor measured about 5 cm, and the bone cortex was thinned and expanded due to tumor growth. Computed tomography (CT) images showed no calcification inside the tumor, and the bone cortex appeared to be partially disrupted. Incisional biopsy showed numerous multinucleated giant cells and no atypical cells, leading to the diagnosis of giant cell tumor of bone (gctb)
Remission Characteristics
A second biopsy showed the almost complete disappearance of multinucleated giant cells and mature bone tissue, with no obvious neoplastic changes or malignant images