We present a case of hypercalcemia in a 79-year-old female likely secondary to uterine leiomyoma. To the best of our knowledge, hypercalcemia due to a benign tumor has only been described in five cases. Of these above five cases, uterine leiomyoma was thought to be the cause of hypercalcemia in three cases.
Hypercalcemia in the setting of a malignancy is a well-defined entity. Hypercalcemia in association with a benign tumor is very uncommon. We present a case of hypercalcemia in a 79-year-old female likely secondary to uterine leiomyoma.
A 79-year-old female was brought to the hospital with altered mental status and acute renal failure after a fall. She was lethargic but had no focal neurologic deficits. Laboratory data was unremarkable except for a serum creatinine of 2.8 mg/dL and serum calcium of 17 mg/dL. She was found to have traumatic subarachnoid hemorrhage for which no acute neurosurgical intervention was thought to be necessary.
Renal ultrasound, serum, and urine protein electrophoresis were unrevealing. Further workup revealed a suppressed parathyroid hormone level of 14 pg/mL (normal: 15–65 pg/mL), 25-hydroxy vitamin D level of 28 ng/mL (normal >32 ng/mL), and an elevated parathyroid hormone related peptide (PTHrP) 40 pg/mL (normal: 14–27 pg/mL). Due to concerns of a malignancy, the patient underwent CT scans of the abdomen and pelvis which revealed multiple punctate calcifications within the uterus thought to be leiomyomas. A CT scan of the thorax was unrevealing. The patient also received a bone scan which did not reveal any areas of osteolytic metastatic disease. Her CA 19-9 and CEA levels were normal but her CA 125 level was elevated at 48 units/mL (<35 units/mL). A transvaginal ultrasound revealed heterogeneously echogenic uterus with multiple ill-defined lesions suggestive of leiomyomas. This was followed by an MRI of the pelvis without contrast which revealed multiple leiomyomas with the dominant one involving the right lateral wall of the uterus.
Her hypercalcemia and renal failure resolved with aggressive hydration and intravenous furosemide.
Hypercalcemia is seen in nearly 20–30 percent of the patients with a malignancy [
Osteolytic bone disease caused by secretion of PTHrP also involves stimulation of osteoclasts that in turn secrete tumour-activating transforming growth factor beta which further stimulates local cancer cells in the setting of metastatic disease [
PTHrP-mediated hypercalcemia associated with a benign tumor is extremely rare and has been described in uterine leiomyoma, dermoid cysts of the ovary, and mammary hyperplasia [
In the case discussed above, the patient was found to have elevated calcium levels in the setting of an elevated PTHrP, suppressed PTH, and a low normal vitamin D level. In the absence of a clear focus of PTHrP secretion, uterine fibroids were presumed to be the likely source. In the cases described earlier in the literature, the authors were able to demonstrate resolution of hypercalcemia with hysterectomy and on one occasion had histologic staining positive for PTHrP [
Thus, uterine leiomyoma should be considered as a possible cause of hypercalcemia mediated through PTHrP in the absence of any other obvious malignancy.
Hypercalcemia is commonly associated with malignancy. Hypercalcemia due to a benign tumor is extremely uncommon. Uterine leiomyoma may be a cause of hypercalcemia and parathyroid hormone related peptide (PTHrP) is thought to be the mediator.