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骨质石化性佝偻病。过量的矛盾。病理生理学与治疗。

Osteopetrorickets. The paradox of plenty. Pathophysiology and treatment.

作者信息

Kaplan F S, August C S, Fallon M D, Gannon F, Haddad J G

机构信息

University of Pennsylvania School of Medicine, Philadelphia.

出版信息

Clin Orthop Relat Res. 1993 Sep(294):64-78.

PMID:8395371
Abstract

Rickets is a common and paradoxical feature of infantile malignant osteopetrosis and results from the inability of osteoclasts to maintain a normal calcium-phosphorus balance in the extracellular fluid. Despite a markedly positive total body calcium balance, rickets arises when the serum calcium x phosphorus product is insufficient to mineralize newly formed chondroid and osteoid. In five children with malignant infantile osteopetrosis, there were clinical, radiographic, biochemical, and histologic findings of rickets. Characteristic biochemical abnormalities included hypocalcemia, hypophosphatemia, and elevated levels of serum acid phosphatase, alkaline phosphatase, c-terminal parathyroid hormone, and 1,25-dihydroxyvitamin D. The urinary calcium/creatinine ratio was markedly depressed. The serum calcium x phosphorus product was below 30 in all children at the time the rickets was diagnosed, and above 40 by the time the rickets had resolved. Baseline bone density measurements were markedly elevated in all children (> 5 standard deviation above normal) and showed even significant increases (> 7 SD) when the rickets was treated with vitamin D and calcium. The children showed marked clinical improvement, decreased lethargy, increase in mobility and activity, and stimulation of appetite, without any additional adverse hematologic or neurologic effects. The rickets was reversible in all children: in one by HLA-identical sibling bone marrow transplantation and in four by physiologic doses of vitamin D and calcium. The parathyroid and renal responses to hypocalcemia were appropriate, but glucocorticoids, used in treating the hematologic complications of the disease, may have blunted the intestinal response to maximal vitamin D stimulation. This latter blockade can be overcome by increasing dietary calcium. By liberalizing rather than by restricting calcium and phosphorus intake, hypocalcemia can be minimized, phosphorus metabolism can be improved, and rickets can be cured.

摘要

佝偻病是婴儿恶性骨硬化症常见且自相矛盾的特征,是由于破骨细胞无法维持细胞外液正常的钙磷平衡所致。尽管全身钙平衡明显呈正向,但当血清钙与磷的乘积不足以使新形成的类软骨和类骨质矿化时,就会出现佝偻病。在5例婴儿恶性骨硬化症患儿中,有佝偻病的临床、影像学、生化和组织学表现。特征性生化异常包括低钙血症、低磷血症以及血清酸性磷酸酶、碱性磷酸酶、甲状旁腺激素C端片段和1,25 - 二羟维生素D水平升高。尿钙/肌酐比值明显降低。在诊断佝偻病时,所有患儿的血清钙与磷的乘积均低于30,而佝偻病消退时则高于40。所有患儿的基线骨密度测量值均明显升高(高于正常5个标准差以上),在用维生素D和钙治疗佝偻病时,骨密度甚至显著增加(超过7个标准差)。患儿临床症状明显改善,嗜睡减轻,活动能力和活动量增加,食欲增强,且无任何额外的血液学或神经系统不良影响。所有患儿的佝偻病均可逆转:1例通过 HLA 相同的同胞骨髓移植,4例通过生理剂量的维生素D和钙实现逆转。甲状旁腺和肾脏对低钙血症的反应是适当的,但用于治疗该疾病血液学并发症的糖皮质激素可能削弱了肠道对最大剂量维生素D刺激的反应。通过增加饮食中的钙可以克服这种后期的阻断作用。通过放宽而非限制钙和磷的摄入,可以将低钙血症降至最低,改善磷代谢,并治愈佝偻病。

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