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Special Feature
August 2001

Pathological Case of the Month

Arch Pediatr Adolesc Med. 2001;155(8):968. doi:10.1001/archpedi.155.8.967
Denouement and Discussion: Classic Rickets in a Setting of Significant Psychosocial Deprivation

Figure 1. Postmortem radiography of the chest and extremities showing enlargements of the costochondral junction in the chest (A) and of the epiphyseal-metaphyseal junctions in the long bones with cupping and fraying of the distal ends (B and C).

Figure 2. Glycol methacrylate bone sections without previous decalcification (A) showing poor removal of cartilage with persistent hypertrophic chondrocytes in the zone of provisional ossification (B), disordered vascular penetration of cartilage with impaired chondrocyte proliferation, and poorly defined broad osteoid seams (C and D). Subperiosteal bone formation is less affected and overtakes endochondral ossification (radiological appearance of the rachitic rosary).

Autopsy revealed poor nutritional status and dwarfism. The external examination showed craniotabes, parietal bossing, and enlargements of distal ends of long bones at the wrist, ankles, elbows, and knees. The lungs showed a consolidation of the parenchyma with infiltrates of neutrophils at the left lower pulmonary lobe, the middle pulmonary lobe, and in both upper pulmonary lobes. Brain examination showed hypoxia signs. The right heart was dilated with hypoxic necrosis of the central regions of the lobules in the liver and hypoxic necrosis of the proximal tubules in the kidney. The cause of death was bilateral pneumonia.

Nutritional rickets affects endochondral and membranous ossification in infants and young children who may have inadequate sunlight exposure coupled with a low dietary intake of vitamin D.1 Rickets owing to vitamin D deficiency develops as a result of the body's attempt to maintain normal serum calcium levels because calcium is necessary for the normal function of nerve, muscle, endocrine glands, and intercellular bridging.2 The lowered calcium level increases the secretion of parathormone, leading to mobilization of calcium and phosphorus from the bone. The serum calcium level is thus maintained, but secondary effects occur, including bone changes, low serum phosphate concentration, and elevated serum alkaline phosphatase. Laboratory values change at advanced stages and during healing.

Clinical signs of rickets include craniotabes, palpable enlargement of the costochondral junctions, and thickening of the wrists and ankles. Diagnosis is based on nutritional history and clinical observation and confirmed by chemical analysis and radiography. Nonrachitic craniotabes can occur in the immediate postnatal period but disappear before rachitic softening of the skull becomes manifest. Congenital epiphyseal dysplasia, cytomegalic inclusion disease, syphilis, rubella, and copper deficiency are further differential diagnoses. In most cases in Western countries, there is a combination of different risk factors, such as maternal vitamin D deficiency, no vitamin D supplementation, long-term breastfeeding, and insufficient sunlight exposure.3 Occult rickets has been reported in Asian immigrant children in the United Kingdom.4 Dagnelie et al5 compared the vitamin D metabolism in white 10- to 20-month-old children receiving a macrobiotic diet with children on omnivorous diets. The low availability of calcium in the macrobiotic diet was an independent factor in causing the high prevalence of rickets in infants with macrobiotic diets.5 Nutritional rickets by child neglect without signs of child abuse has received little attention.6 The mother of this patient was an alcoholic; alcohol abuse is present in many families with abused or neglected children. In these families, marital problems, unemployment, and drug abuse may play a role as trigger factors.7,8 Prevention and treatment measures for problems related to alcohol have been proposed, such as home visitation services.

Pneumonia is an important complication of rickets in developing countries. In Iran, 43% of 200 children with radiologically proven rickets had bronchopneumonia,9 44% of 250 Kuwaiti children with vitamin D deficiency rickets had pneumonia,10 and 44 (81%) of 54 Egyptian children with rickets had acute respiratory infections.11 Muhe et al12 found a 13-fold higher incidence of rickets among children with pneumonia than among controls. The association of rickets and pneumonia may be explained by effects of the hormonal form of vitamin D (calcitriol) on the immune system. Calcitriol stimulates phagocyte-dependent and antibody-dependent macrophage cytotoxicity and modulates functions of T and B lymphocytes.13 Constitutional factors, including the Harrison groove and atelectasis, may also contribute to pneumonia in children with vitamin D deficiency.

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Article Information

Accepted for publication August 25, 1999.

Reprints: Consolato Sergi, MD, Institute of Pathology, University of Heidelberg, INF 220/221, D-69120 Heidelberg, Germany (e-mail: Consolato_Sergi@med.uni-heidelberg.de).

References
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Lawson  DECole  TJSalem  SI  et al.  Etiology of rickets in Egyptian children. Hum Nutr Clin Nutr. 1987;41199- 208
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Muhe  LLulseged  SMason  KESimoes  EA Case-control study of the role of nutritional rickets in the risk of developing pneumonia in Ethiopian children. Lancet. 1997;3491801- 1804Article
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Lemire  JMAdams  JSKermani-Arab  V  et al.  1,25-Dihydroxyvitamin D3 suppresses human T helper/inducer lymphocyte activity in vitro. J Immunol. 1985;1343032- 3035
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