keyword
https://read.qxmd.com/read/37350024/phosphaturic-mesenchymal-tumor-a-chondromyxoid-fibroma-like-type
#1
JOURNAL ARTICLE
Kaori Koga, Hiroshi Iwasaki, Kazuki Nabeshima
Phosphaturic mesenchymal tumor (PMT) is a rare neoplasm that causes tumor-induced osteomalasia (TIO) in most affected patients, usually through the production of fibroblast growth factor 23 (FGF23). This tumor is often misdiagnosed due to its relative rarity and its widely varied histomorphologic spectrum. Here we describe a case of a 78-year-old woman who presented with a left middle tumor without symptoms of TIO. The histological features resembled chondromyxoid fibroma with smudgy calcification in the tumor matrix...
June 22, 2023: Journal of Dermatology
https://read.qxmd.com/read/33446319/nasal-hemangiopericytoma-presenting-with-oncogenic-osteomalasia-a-case-report-and-literature-review
#2
Ali Gökyer, Sezin Sayın, Ahmet Küçükarda, Mehmet Çelik, Sibel Güldiken, İrfan Çiçin
Sinonasal type hemangiopericytoma is a rare soft tissue tumor. Oncogenic osteomalacia (tumor-induced osteomalacia) is a rare syndrome that develops especially due to benign mesenchymal tumors. Nonspecific general bone pain and weakness delay the diagnosis and treatment of oncogenic osteomalacia, and it is difficult to determine the localization of the primary tumor causing oncogenic osteomalacia. A 43-year-old male patient with nasal hemangiopericytoma with symptoms of oncogenic osteomalacia is presented. The patient had musculoskeletal complaints at first and was diagnosed with lumbar disc herniation and surgery was performed...
January 8, 2021: Current Problems in Cancer
https://read.qxmd.com/read/15577031/-treatment-of-bone-disease-in-chronic-kidney-disease-and-in-renal-transplant-recipients-under-k-doqi-clinical-practice-guidelines
#3
REVIEW
Tadahiko Tokumoto, Kazunari Tanabe, Hiroshi Toma, Takashi Akiba
The National Kidney Foundation's Kidney Disease Outcomes Quality Initiative (K/DOQI) provides evidence based clinical practice guidelines developed for all phases of kidney disease and related complications, from diagnosis to monitoring and management. Bone disease sets in during the early stages of Chronic Kidney Disease (CKD). Bone disease is observed in almost patients with chronic renal failure and after renal transplantation. Hyperparathyroid (high turnover) bone disease in patients with chronic renal failure is found most frequently followed by mixed osteodystrophy, low-turn over bone disease, and osteomalasia...
May 2004: Clinical Calcium
https://read.qxmd.com/read/8587212/-renal-disease-and-trace-elements
#4
REVIEW
F Marumo, J P Li
Correlation between renal disease and trace elements includes following two types; 1) Renal failure due to excess of trace element intake into the body, such as itai-itai disease or heavy metal intoxication. 2) Disturbances of trace elements in patients with chronic renal failure, such as aluminum dementia and aluminum-related bone disease. Itai-itai disease occurred by water pollution with cadmium. Cadmium causes Fanconi syndrome in the kidney and osteomalasia in person, especially in old women, who were living near the riverside...
January 1996: Nihon Rinsho. Japanese Journal of Clinical Medicine
https://read.qxmd.com/read/1609662/-clinical-study-of-parathyroidectomy-of-secondary-hyperparathyroidism-in-patients-with-chronic-renal-failure
#5
JOURNAL ARTICLE
S Yamaguchi, S Yachiku, M Morikawa, M Okuyama, A Numata, F Inada, T Anzai, T Kobayashi, K Furuta, H Ishida
We performed parathyroidectomy for renal osteodystrophy due to secondary hyperparathyroidism on 16 patients with chronic renal failure who were refractory to medical management; subtotal parathyroidectomy on one patient and total parathyroidectomy with autotransplantation on 15 patients. Postoperative clinical improvement, i.e., bone and/or joint pain, pruritus and radiographic signs of renal osteodystrophy, was marked. After the operation, serum calcium decreased rapidly and adequate calcium replacement therapy was necessary...
May 1992: Hinyokika Kiyo. Acta Urologica Japonica
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