Diagnosis and surgical treatment of tumor-induced osteomalacia—a literature review and a case report

نویسندگان

چکیده

Abstract Background Tumor-induced osteomalacia (TIO) is a rare condition with fewer than 500 cases reported in the literature although described. Phosphaturic mesenchymal tumor (PMT) often unrecognized cause of hypophosphatemia. This case report aims to highlight such association which warrants clinical and radiologist attention. Case A 51-year-old man had pain his feet 2 years prior most recent presentation our clinic. The patient experienced increasingly severe body aches pain, affected feet, hips, knees, ribs, waist, shoulders. MRI CT led diagnosis multiple insufficiency fractures. Laboratory tests showed that inorganic phosphate (IP) levels decreased 0.52 mmol/L(0.81–1.45 mmol/L), while alkaline phosphatase (ALP) increased 216 U/L(38.0–126.0 U/L). Positron emission tomography computed tumor-derived hypophosphate right iliac wing; surgical resection was performed. markers bone metabolism density returned normal postoperative, after 9 months follow-up. Conclusion possibility tumor-induced should be considered if unexplained joint mineral density, ALP fractures, no similar family history are found adult patients. Surgical key treatment.

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

TUMOR ASSOCIATED OSTEOMALACIA IN NEUROFIBROMATOSIS: CASE REPORT AND LITERATURE REVIEW

The association of osteomalacia with neurofibromatosis is a very rare entity. Here a 34 year old man, a known case of neurofibromatosis, is reported who presented with bone pain, hypophosphatemia, rena] phosphorus wasting, multiple Looser's pseudofractures, and low bone density. Treatment with high dose calcitriol and phosphate resulted in temporary treatment. Permanent cure was achieved a...

متن کامل

Postpartum Hypercalcemia Secondary to a Neuroendocrine Tumor of Pancreas; a Case Report and Review of Literature

Parathyroid hormone-related protein producing pancreatic neuroendocrine tumors have been infrequently reported. Herein, we report a case of an Iranian woman who had such a tumor during pregnancy, and gave birth to a female neonate with esophago-tracheal fistula and imperforated anus. Hypercalcemia was diagnosed at postpartum because of elevated serum calcium levels in the neonate and neurologic...

متن کامل

Solid Pseudopapillary Tumor of the Pancreas: a Case Report and Literature of Review

Solid pseudopapillary tumors of the pancreas (SPT) are rare tumors of the pancreas with low malignancy potential and a very good prognostic outcome after surgery. The outcome after radical resection is favourable. A case of solid-pseudopapillary tumor (SPT) of the pancreas in a 20-year-old woman is presented. The patient underwent resection of the mass in the pancreatic head and pancreaticoduod...

متن کامل

A novel case of quartet tumor: meningioma, angiomyolipoma, ependymoma and sarcoma: report of a case and review of the literature

Multiple primary tumors in a single patient are relatively rare when four or more distinct lesions are considered. Herein, we report a case of woman with four different primary tumors: meningioma, renal angiomyolipoma, spinal ependymoma and high-grade soft tissue sarcoma. There was no family history and hereditary syndrome. The genetic analysis was completely normal. To best of our knowledge, t...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: The Egyptian Journal of Internal Medicine

سال: 2022

ISSN: ['1110-7782', '2090-9098']

DOI: https://doi.org/10.1186/s43162-022-00101-3