A CASE OF SEVERE HYPERCALCAEMIA SECONDARY TO PARATHYROID CARCINOMA

INTRODUCTION Parathyroid carcinoma is a rare malignancy, accounting for only 0.005% of all cancers and about 0.5-1% of parathyroid disorders with similar incidence in male and females. It usually presents with manifestations of severe hypercalcaemia with bone involvement and nephrolithiasis, associated with markedly raised parathyroid hormone; although presentations can be variable. CASE We report a case of a 44-year-old Chinese male with underlying hypertension, chronic kidney disease stage 3A (eGFR 52 mL/min/1.73 m2) who was incidentally found to have PTH–dependent severe hypercalcaemia (corrected calcium 4.56 mmol/L), hypophosphataemia with iPTH 102.1 (>7 times the upper limit of normal) during admission for left cheek subcutaneous abscess. Hypercalcaemia was managed with calcitonin, bisphosphonate alongside aggressive saline diuresis resulting to a serum calcium of 2.85 mmol/L. Ultrasound of the neck showed a well-defined ovoid hypoechoic lesion, caudal to the lower pole of the left thyroid lobe measuring 1.4 x 1.5 x 2.0 cm consistent with left parathyroid adenoma, which was confirmed with parathyroid Sestamibi scintigraphy. Ultrasound of the kidneys revealed no nephrolithiasis while bone densitometry showed severe osteoporosis at the distal third of forearm and left neck of femur with T score -4.1 and 3.0 respectively. Surgical excision of the left parathyroid with intraoperative PTH monitoring was done with subsequent removal of the lesion leading to normalization of the PTH level. Histopathology examination revealed lymphovascular permeation with irregular nodular proliferation of parathyroid cells with transgressed boundaries which are features compatible with parathyroid carcinoma. Post operatively, the patient was normocalcaemic but declined further surgical tumour clearance. CONCLUSIONThis case highlights the need for a high index of clinical suspicion for the presence of parathyroid carcinoma pre-operatively in patients who exhibit severe hypercalcemia, markedly raised PTH and bone manifestations so that en bloc-resection of the parathyroid with ipsilateral partial thyroidectomy and central node dissection can be planned prior to surgery.

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Publication Details

Journal
Journal of the ASEAN Federation of Endocrine Societies
Published
2025-05-30
DOI
https://doi.org/10.15605/jafes.040.s1.012
Primary Topic
Bone and Joint Diseases
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article
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article

A CASE OF SEVERE HYPERCALCAEMIA SECONDARY TO PARATHYROID CARCINOMA

Meng Loong Mok, Shireene Ratna Vethakkan, Abdullah Shamshir Abd Mokti
Journal of the ASEAN Federation of Endocrine Societies
Bone and Joint Diseases
article

A CASE OF SEVERE HYPERCALCAEMIA SECONDARY TO PARATHYROID CARCINOMA

Meng Loong Mok, Shireene Ratna Vethakkan, Abdullah Shamshir Abd Mokti
article en

Abstract

INTRODUCTION Parathyroid carcinoma is a rare malignancy, accounting for only 0.005% of all cancers and about 0.5-1% of parathyroid disorders with similar incidence in male and females. It usually presents with manifestations of severe hypercalcaemia with bone involvement and nephrolithiasis, associated with markedly raised parathyroid hormone; although presentations can be variable. CASE We report a case of a 44-year-old Chinese male with underlying hypertension, chronic kidney disease stage 3A (eGFR 52 mL/min/1.73 m2) who was incidentally found to have PTH–dependent severe hypercalcaemia (corrected calcium 4.56 mmol/L), hypophosphataemia with iPTH 102.1 (>7 times the upper limit of normal) during admission for left cheek subcutaneous abscess. Hypercalcaemia was managed with calcitonin, bisphosphonate alongside aggressive saline diuresis resulting to a serum calcium of 2.85 mmol/L. Ultrasound of the neck showed a well-defined ovoid hypoechoic lesion, caudal to the lower pole of the left thyroid lobe measuring 1.4 x 1.5 x 2.0 cm consistent with left parathyroid adenoma, which was confirmed with parathyroid Sestamibi scintigraphy. Ultrasound of the kidneys revealed no nephrolithiasis while bone densitometry showed severe osteoporosis at the distal third of forearm and left neck of femur with T score -4.1 and 3.0 respectively. Surgical excision of the left parathyroid with intraoperative PTH monitoring was done with subsequent removal of the lesion leading to normalization of the PTH level. Histopathology examination revealed lymphovascular permeation with irregular nodular proliferation of parathyroid cells with transgressed boundaries which are features compatible with parathyroid carcinoma. Post operatively, the patient was normocalcaemic but declined further surgical tumour clearance. CONCLUSIONThis case highlights the need for a high index of clinical suspicion for the presence of parathyroid carcinoma pre-operatively in patients who exhibit severe hypercalcemia, markedly raised PTH and bone manifestations so that en bloc-resection of the parathyroid with ipsilateral partial thyroidectomy and central node dissection can be planned prior to surgery.

Journal of the ASEAN Federation of Endocrine SocietiesVol. 40(S1)
Openalex Percentile: Top 84%
Bone and Joint Diseases
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