A Case Report of Treatment of Heterotrophic Calcification in Pseudohypoparathyroidism.
- Author:
Sung Won YOON
1
;
Jea Yong SONG
;
Chung Hun KIM
Author Information
1. Department of Plastic and Reconstruction Surgery, School of Medicine, CHA University, Gyeonggi-do, Korea. iicharmi@hanmail.net
- Publication Type:Case Report
- Keywords:
Pseudohypoparathyroidism;
Heterotrophic calcification
- MeSH:
Basal Ganglia;
Biopsy;
Brain;
Calcium;
Cerebellar Nuclei;
Dermis;
Epilepsy;
Female;
Fibrous Dysplasia, Polyostotic;
Foot;
Humans;
Hypoparathyroidism;
Pseudohypoparathyroidism;
Reference Values;
Stress, Psychological;
Subcutaneous Tissue;
Surgery, Plastic;
Thyroid Gland;
X-Ray Film;
Young Adult
- From:Journal of the Korean Society of Plastic and Reconstructive Surgeons
2010;37(3):281-284
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
PURPOSE: Pseudohypoparathyroidism is a hereditary disorder characterized by symptoms and signs of hypoparathyroidism, typically in association with distinctive skeletal and developmental defects. Hypoparathyroidism is caused by a insufficient end-organ response to PTH (parathyroid hormone). Hypoparathyroidism consists of four types in which the most common form, pseudohypoparathyroidism-Ia, accompany with Albright's hereditary osteodystrophy. We experienced a case of a woman who had been suffering from calcified mass on left foot, diagnosed Albright's hereditary osteodystrophy. METHODS: We present a case of a 24-year-old Korean female who visited plastic surgery department with a painful mass on dorsum of the left foot. On the physical exam, bony hard and painful mass, fixed to dermis, was noted. Plain X-ray films demonstrate suspicious calcification on subcutaneous tissue of dorsum of the left foot. The patient was diagnosed pseudohypoparathyroidism 2 years ago at the plastic surgery department. At the visiting time, the laboratory results were within normal range even though the patient actually had a disease. The reason is because the patient has been treated with Vit.D, calcium replacement therapy and thyroid hormone therapy. Moreover, the patient has been treated with anticonvulsant agents due to epilepsy. On the brain computer tomography (CT), calcification was noted on the basal ganglia and dentate nucleus. So we decided the total excision of entire mass from the left foot. RESULTS: We excised main mass with numerous pinhead sized masses which were scattered around the main mass. The 6.0x4.0x0.5 cm sized main mass was bony hard, and its surface was flat and margin was irregular. The permanent biopsy was confirmed that the main mass and all the scattered tiny masses were heterotopic calcification. The patient did not suffer from the pain after the mass excision. The wound has been healed without any problem. CONCLUSIONS: Heterotrophic calcification is often accompanied with pseudohypoparathyroidism, but such a huge one is uncommon. We report a case of pseudohypoparathyroidism with heterotrophic calcification developed in dorsum of left foot who was diagnosed by excisional biopsy.
