Mittal Rajneesh, Kalra Pramila, Dharmalingam Mala
Department of Endocrinology, MS Ramaiah Medical College, Bangalore, Karnataka, India.
Indian J Endocrinol Metab. 2012 Dec;16(Suppl 2):S413-5. doi: 10.4103/2230-8210.104112.
Osteomalacia is one of the most common osteometabolic diseases. It is typically caused by lack of vitamin D and is characterized by mineralization deficiency of the osteoid matrix in the cortical and trabecular bone. Indians are at particularly high risk for developing osteomalacia, because of their traditional clothing style and skin color. This condition is frequently misdiagnosed and it can present with bone pain and muscle weakness.
We report a case of osteomalacia with predominant hypophosphatemia.
A 41-year-old male presented with gradually progressive quadriparesis for past 6 months. Patient had low phosphorous (1.9 mg/dl) with calcium being 8.1 mg/dl and 25(OH)Vitamin D3 levels being 8.12 ng/ml. The patient was thought to have concomitant Vitamin D deficiency with possibility of tumor-induced osteomalacia. Further evaluation for the same was planned. However, patient was given a trial of Vitamin D supplementation before further investigations and had dramatic improvement in the form that muscle power improved gradually over next 6 weeks and was able to climb stairs after 2 months. Retrospectively patient gave a history of being at home for many months and there was no exposure to sunlight at all. The biochemical parameters normalized within 4 weeks of starting Vitamin D and serum alkaline phosphatase showed drastic reduction after 6 weeks. All his family members were screened and found to have Vitamin D deficiency including recent born twins having rachitic changes. This was a case of vitamin D deficiency, in 41-year-old male, which presented more like hypophosphatemic osteomalacia but characteristic history of lack of sunlight exposure and dramatic improvement with only vitamin D3 supplementation confirmed the diagnosis.
The presentation of vitamin D deficiency can be varied and high index of suspicion is important for treatment of this common but frequently misdiagnosed condition.
骨软化症是最常见的骨代谢疾病之一。它通常由维生素D缺乏引起,其特征是皮质骨和小梁骨中类骨质基质的矿化不足。由于传统的着装风格和肤色,印度人患骨软化症的风险特别高。这种疾病经常被误诊,可表现为骨痛和肌肉无力。
我们报告一例以低磷血症为主的骨软化症病例。
一名41岁男性在过去6个月中出现逐渐进展的四肢无力。患者血磷低(1.9mg/dl),血钙8.1mg/dl,25(OH)维生素D3水平8.12ng/ml。患者被认为同时存在维生素D缺乏,可能患有肿瘤诱导的骨软化症。计划对此进行进一步评估。然而,在进一步检查之前,先对患者进行了维生素D补充试验,结果患者有显著改善,表现为在接下来的6周内肌肉力量逐渐增强,2个月后能够爬楼梯。回顾病史,患者在家中待了数月,完全没有阳光照射。开始补充维生素D后4周内生化指标恢复正常,6周后血清碱性磷酸酶大幅下降。对其所有家庭成员进行筛查,发现均存在维生素D缺乏,包括最近出生的双胞胎有佝偻病改变。这是一例41岁男性维生素D缺乏病例,其表现更像低磷性骨软化症,但缺乏阳光照射的典型病史以及仅补充维生素D3后显著改善证实了诊断。
维生素D缺乏的表现可能多种多样,对于这种常见但经常被误诊的疾病,高度的怀疑指数对于治疗很重要。