Histological examination of the bones obtained on autopsy of a 5-month-old child with mucolipidosis II (I-cell disease) revealed inhibition of the growth plate calcification with defective vascular invasion and signs of hyperparathyroidism. These findings are the chondro-osseous basis of the early radiological ricket-like appearance of bones in the neonatal period or soon thereafter. Whether the early skeletal abnormalities of mucolipidosis II result from a primary enzymatic defect of cartilage and bone cells or from factors controlling bone metabolism deserves further study

Beluffi G

Bianchi E

Castello A

Coci A

Marchi A.

Pazzaglia U

PAZZAGLIA, Ugo

Archivio istituzionale della ricerca - Università di Brescia

Eur J Pediatr (1989) 148: 553-557 European Journal of Pediatrics 9 Springer-Verlag 1989 Study of the bone pathology in early mucolipidosis II (1-cell disease) U. E. Pazzaglia 1, G. Belutli 2 , E. Bianchi 3, A .  Castello 4 , A .  Coci 4, and A.  Marchi 3 t Clinica Ortopedica e Traumatologica dell'Universitfi di Pavia, and 2 Servizio di Radiodiagnostica, I.R.C.C.S. Policlinico San Matteo, Via Taramelli 3, 1-27100 Pavia, Italy 3Clinica Pediatrica dell'Universitfi di Pavia, Pavia, Italy 4Dipartimento di Patologia Umana ed Ereditaria, Sezione di Anatomia Patologica, Pavia, Italy Abstract. Histological examination of the bones obtained on autopsy of a 5-month-old child with mucolipidosis II (I-cell disease) revealed inhibition of the growth plate calcification with defective vascular invasion and signs of hyperparathy- roidism. These findings are the chondro-osseous basis of the early radiological ticket-like appearance ofbones in the neonatal period or soon thereafter. Whether the early skeletal abnor- malities of mucolipidosis II result from a primary enzymatic defect of cartilage and bone cells or from factors controlling bone metabolism deserves further study. Key words: Mucolipidosis II - I-cell disease - Dysostosis multiplex - Rickets - Hyperparathyroidism Introduction Dysostosis multiplex is a constant finding in mucolipidosis II. The progression of the skeletal abnormalities with age [2, 5, 7, 8] may result from the same storage process in bone cells as in viscera or from the effect of factors controlling bone turn- over. No evidence supporting either of these hypotheses has been presented and few histological studies of bone are avail- able [1, 3, 6, 9, 10]. We describe a child with I-cell disease, who died at 5 months of age and report a detailed study of the bone alterations. Case report The patient born on 17 January 1986, was the second son of first cousins whose first son was normal. The family history was negative, The child was born at 38 weeks of gestation. The birth weight was 2800g and weight gain in the first 2 months was reported to be normal. He was admitted for the first time at the age of 2 mouths because of a left hydrocele. The following physical findings were observed: micro- cephalus, hypertelorism, low-set ears, high-arched palate, hypertrophic gums, generalized muscle hypotonia, breathing difficulty. A skeletal survey showed generalized osteoporosis with coarse, lacy trabeculae and a spongy appearance of diaphyseal cortical bone. Periosteal thickening, cupping and irregularity of the metaphyses were evident in the long bones. High values of serum alkaline phosphatase (2950, 3130, 2810, 2098 U/l) were repeatedly observed. Serum calcium and phos- Offprint requests to: U. E. Pazzaglia phate were low (Ca from 6.6 to 8.46 mg/dl and PO4 from 2.21 to 3.82 mg/dl), urinary calcium was low, while phosphate was high. Serum parathyroid hormone level was elevated (1.7 pg/ ml). The only other abnormalities were mild leukocytosis and hypochromic anaemia. A diagnosis of skeletal dysplasia with hypophosphataemic rickets was made and treatment with vita- min D (50,000 IU/day) and sodium phosphate (1 g/day) was started. Following therapy no improvement was observed. At the age of 5 months the child was admitted to the Paediatric Department of the University of Pavia. Weight was 3830 g (< 10th percentile); height 56.6 cm (< 10th percentile); head circumference 4i cm (< 10th percentile). The baby's general condition was poor with pale skin, hypotrophic mus- cles and scanty subcutaneous tissue. The anterior fontanelle was 0.5 cm • 1 cm. The child had no teeth and the gums were markedly hypertrophic; the nostrils were anteverted. The chest was funnel shaped, the sternum bowed and the costo- sternal junctions were hypertrophic. Heart sounds were nor- mal, the liver was palpable 3cm below the costal margin, Small superficial ymph nodes were present. Routine laboratory tests were normal except for leukocytosis and hypochromic anaemia. Alkaline phosphatase was 1747mU/ml (normal range 120-700 mU/ml) and serum phosphate 6.63 mg/dl (nor- mal range 4-7 mg/dl). Amino acids and glucose were absent in the urine. The child died before parathyroid hormone levels could be determined. Skin fibroblasts were cultured and lysosomal enzymes were assayed in plasma, leukocytes and fibroblasts (Table 1). Cultured fibroblasts howed characteristic cytoplasmic inclu- sions. Table 1. Levels of acid hydrolases in plasma, leucocytes and fibro- blasts Acid hydrolases Plasma Fibroblasts Arylsulphatase A 84.45 A/ml/h (1.44) Totalhexosaminidases 14727 A/ml/h (735.43) ~-galactosidase a-mannosidase 14.85-23.92 A/mg/h (150-500) 393.07-854.57 A/mg/h (3000-10000) 11.34-11.84 A/mg/h (300-800) 13.26-14.09 A/mg/h (54.8-120.7) ( ) = control values Arylsulphatases A activity in leucocytes was 95% of controls (not sig- nificant) 554 Fig. 1. Radiographic appearance. Lower limbs: frayed metaphyses with a sclerotic horizontal line; the proximal metaphyses of the tibiae have a medial to lateral tapering, while the proximal left femur is bent medially; cloaking of diaphyses i  evident in the tibiae. Small flecks of calcium are present below the irregular nucleus of the astragalus; cupped, rachitic-like appearance of the distal tibia and fibula. Spine and upper limbs: osteopenia, bnormal trabecular pattern and cloaking of tubular bones; a cupped, ticket-like aspect of metaphysis is particularly evident in the distal radius; bullet- shaped phalanges in the hands Radiographic findings Bone survey showed generalized osteopenia with the excep- tion of the bones of the base of the skull which were thickened and sclerotic. Maxilla and mandible were undermineralized and the teeth seemed to float within the poorly textured bone. The long bones were osteoporotic with enlarged medullary canals, coarsely structured with thin trabeculae and a cloak- like appearance of the entire shaft of the tubular bones of the lower limbs. The metaphyses of the long bones were frayed and those of the distal ulnae, radii, tibiae and fibulae also cup- ped with submetaphyseal bone resorption which in the distal femurs and proximal tibiae was limited by a sclerotic horizon- tal line (Fig. 1). The scapulae were poorly calcified and mis- shapen with an irregular texture and shallow glenoid cavities; the clavicles were deformed and the ribs short and broad with cup-like distal ends. Narrowing of the interpeduncular dis- tance in the lower thoracic spine was present. In the lateral view, ovoid vertebral bodies with some anterior beaking of the first and second lumbar vertebrae were associated with a dorso-lumbar kyphosis (Fig. 1). Other findings were proximal pointing of metacarpal bones, brachyphalangy with bullet- shaped phalanges (Fig. 1), stippling of the tarsus, flared iliac wings, and a horizontal acetabular roof with supra-acetabular constriction. The bone changes had progressed compared to films taken 2 months earlier where bone rarefaction was already present but signs of sub-periosteal resorption less evident. Pathology Autopsy was performed 24 h after death. The following bones were studied: right tibia, 4th, 5th and 6th right ribs, 4th, 5th 555 Fig. 2. X-rays of the right tibia and general histological view (haematoxylin- eosin, 2.5 x): squareA, B, and C correspond to Figs. 3, 5 and 6 and 6th dorsal vertebrae and sternum. All bones examined were softer than normal. The growth plate had abnormally high columnar and hyper- trophic cell layers (Fig. 2). Staining of the cartilage matrix with PAS and Alcian blue was normal but the intercolumnar septa were not calcified (Fig. 3). The metaphyseal side of the growth plate was very irregular; normal vascular invasion was lacking, while large buds of fibrous tissue penetrated from the mataphysis into the cartilage, giving an indented appearance at low magnification. Osteoid deposition was disorderly. Osteoclasts were numerous (Fig. 4). Large vacuoles were oc- casionally observed in swollen fibroblasts. Primary metaphyseal trabeculae were lacking; the few sec- ondary trabeculae had undergone intense remodelling and ap- peared surrounded by several layers of fibrous tissue (Fig. 5). Beneath the periosteum the bone consisted of very thin lamellae; more than 3/4 of the full thickness of the cortex was occupied by loose vascular connective tissue. Many osteoclasts were observed in each field but new bone was also being layed down by active osteoblasts (Fig. 6). Autopsy confirmed multiple foci of bronchopneumonia with gray hepatization of the lungs. A few vacuolated macro- phages were observed in the alveolar walls. The liver was increased in volume and congested and many hepatocytes had vacuoles in the cytoplasm. Clear, cytoplasmic inclusions were also observed in the glomerular and epithelial cells of the proximal convoluted tubules of the kidney. Para- thyroids glands were not found. Discussion The clinical and radiographic features of this case are those of mucolipidosis II [2, 5, 7, 8]. The diagnosis was made on the basis of the decreased acid hydrolase activity in cultured fibro- blasts and an increase of acid hydrolases in plasma. 556 Fig. 3. Abnormally high columnar and hypertrophic cell layers of the growth plate cartilage and failure of intercolumnar septa calcification (von Kossa, 100 • Few studies describe the pathology of bones in detail. Mar- tin et al. [6] observed a marked disturbance of endochondral ossification with disarray of the proliferative and hypertrophic cell layers in an 8.5-months-old girl. Growth arrest of the epi- physeal plate and lack of the normal columnar arrangement was reported by Gilbert et al. [3] in three older children (aged 2, 6 and 8 years). In a 19-week fetus, Babcock et al. [1] observed decreased bone mineralization, a coarse trabecular pattern, shortened and under-modelled bones and sub-periosteal bone deficiency. The hypothesis common to all these studies is that the enzymatic defect in osteogenic cells may interfere directly with new bone deposition. Ricket-like lesions and signs of hyperparathyroidism were present in our patient. Similar radiographic hanges have been observed in other neonatal cases of mucolipidosis II [2, 5, 7]. Hypophosphataemic rickets was suspected at the age of 2 months on the basis of the high levels of serum alkaline phosphatase, hypophosphataemia and hyperphosphaturia. Whether hyperparathyroidism was secondary to hypophos- phataemic rickets cannot be established from the data avail- able. Dysostosis developed later and was superimposed on the radiographic appearance of rickets. The pathogenesis of dys- 5 Fig. 4. The abnormal pattern of the growth-plate cartilage and metaphysis with rickets-like f atures (haematoxylin-eosin, 250 • Fig. 5. Metaphyseal trabeculae are surrounded by several layers of fibrous tissue as is usually seen in hyperparathyroidism (haematoxylin-eosin, 250 x) 557 Fig. 6, Subperiosteal resorption is responsible for the cioaking-like aspects een in X-rays. The full thickness of the cortex is undergoing fast re- modelling (P = periosteum; arrows indicate osteoclasts) (haematoxylin-eosin, 100 • ostosis multiplex is not clear but appears to be related to the defective lysosomal enzyme activity. Mucolipidosis II is caused by defective processing of hydrolases which interferes with their entrance into lysosomes [4]. Based on experience with the other mucolipidoses and mucopolysaccharidoses this defect explains dysostosis multi- plex but not the inhibition of calcification, ricket-like features and hyperparathyroidism observed in this infant with muco- lipidosis II. Cause of the defective mineralization and its relationship to the primary defect in neonatal mucolipidosis II remains obscure and deserves further study. Acknowledgements. The authors wish to thank Prof. C. Danesino for the skin fibroblast culture and the acid hydrolase determination and Dr. V. Monaf6 who reviewed the English text. References 1. Babcock DS, Bove KE, Hug G, Dignan PSJ, Soukup S, Warren WS (1986) Fetal mucolipidosis II (I-cell disease): radiologic and pathologic correlation. Pediatr Radiol 16 : 32-39 2. Baggio P (1978) I-cell disease. Mucolipidosi II o Sialidosi. Min Ped 30 : 865-884 3. Gilbert EF, Dawson G, Zu Rhein GM, Opitz JM, Spranger JW (1973) I-cell disease, mucolipidosis II. Histochemical Ultrastruc- tural and biochemical observations in four cases. Z Kinderheilkd 114:259-292 4. Hickman S, Neufeld EF (1972) A hypothesis for I-cell disease: de- fective hydrolases that do not enter lysosomes. Biochem Biophys Res Commun 49 : 992-999 5. Lemaitre L, Remy T, Farriaux JP, Dhondt JL, Walbaum R (1978) Radiological signs of mucolipidosis II or I-cell disease. Pediatr Radiol 7: 97-105 6. Martin JJ, Leroy JG, Farriaux JP, Fontaine G, Desnick RJ, Cabello A (1975) I-cell disease (mucolipidosis II). A report on its pathology. Acta Neuropathol (Berl) 33 : 285-305 7. Patriquin HB, Kaplan P, Kind HP, Giedion A (1977) Neonatal mucolipidosis II (I-cell disease): clinical and radiological features in three cases. Am J Roentgenol 129 : 37-43 8. Taber P, Gyepes MT, Phillippart M, Ling S (1975) Roentgenog- raphic manifestation of Leroy's I-ceil disease. Am J Roentgenol 118:213-221 9. Terashima Y, Tsuda K, Isomura S, Sugiura Y, Nogami H (i975) I-cell disease. Am J Dis Child 129 : 1083-1090 10. Tondeur M, Vamos-Hurwitz E, Mockel-Pohl J, Dereume JP, Cremer N, Loeb H (197t) Clinical, biochemical and ultrastruc- tural studies in a case of chondrodystrophy presenting the I-cell phenotype in tissue culture. J Pediatr 79 : 366-378 Received January 21, 1988 / Accepted August 16, 1988 

Study of the bone pathology in early mucolipidosis II (I-cell disease).

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