Subscribe to RSS
DOI: 10.1055/s-2005-918892
Nonimmune Hydrops Fetalis Due to Generalized Lymphatic Dysplasia in an Infant with Robertsonian Trisomy 21
Publication History
Publication Date:
04 November 2005 (online)
ABSTRACT
We report the first case of generalized lymphatic dysplasia and trisomy 21 presenting with nonimmune hydrops fetalis. This infant showed intractable chylothorax, chylous ascites, and periodic bouts of edema. A karyotype analysis revealed Robertsonian trisomy 21: 46,XY,t(14q21q)(q10;q10) +21. This patient died of multiple organ failure at 400 days of life, despite the management of chylous effusions. The lymphoscintigraphy and histopathological findings led to the final diagnosis of generalized lymphatic dysplasia, which might also contribute to the development of hydrops. Refractory chylothorax in trisomy 21 patients may emphasize the need for intensive scrutiny of lymphatic disorders.
KEYWORDS
Lymphatic diseases - Robertsonian trisomy 21 - chylothorax
REFERENCES
- 1 Puddy V, Lam B CC, Tang M et al.. Variable levels of mosaicism for trisomy 21 in a non-immune hydropic infant with chylothorax. Prenat Diagn. 1999; 19 764-766
- 2 Turan O, Canter B, Ergenekon E, Koc E, Atalay Y. Chylothorax and respiratory distress in a newborn with trisomy 21. Eur J Pediatr. 2001; 160 744-745
- 3 Behrman R E, Kliegman R M, Jenson H B. Nelson Textbook of Pediatrics, 16th ed. Philadelphia; WB Saunders 2000
- 4 Smeltzer D M, Stickler G B, Fleming R E. Primary lymphatic dysplasia in children: chylothorax, chylous ascites, and generalized lymphatic dysplasia. Eur J Pediatr. 1986; 145 286-292
- 5 Podevin G, Levard G, Larroquet M, Gruner M. Pleuroperitoneal shunt in the management of chylothorax caused by thoracic lymphatic dysplasia. J Pediatr Surg. 1999; 34 1420-1422
- 6 Guttman F M, Montupet P, Bloss R S. Experience with peritoneo-venous shunting for congenital chylous ascites in infants and children. J Pediatr Surg. 1982; 17 368-372
- 7 Man D W, Spitz L. The management of chylous ascites in children. J Pediatr Surg. 1985; 20 72-75
- 8 Bloomfield F, Hadden W, Gunn T R. Lymphatic dysplasia in a neonate with Noonan's syndrome. Pediatr Radiol. 1997; 27 321-323
- 9 Lanning P, Simila S, Suramo I, Paavilainen T. Lymphatic abnormalities in Noonan's syndrome. Pediatr Radiol. 1978; 7 106-109
- 10 Hilliard R I, McKenobey J BJ, Phillips M J. Congenital abnormalities of the lymphatic system: a new clinical classification. Pediatrics. 1990; 86 988-994
- 11 Oliver G. Lymphatic vasculature development. Nat Rev Immunol. 2004; 4 35-45
- 12 Jain R K, Padera T P. Lymphatics make the break. Science. 2003; 299 209-210
- 13 Abtahian F, Guerriero A, Sebzda E et al.. Regulation of blood and lymphatic vascular separation by signaling proteins SLP-76 and Syk. Science. 2003; 299 247-251
- 14 Karkkainen M, Ferrel R E, Lawrence E C et al.. Missense mutation interfere with VEGFR-3 signaling in primary lymphoedema. Nat Genet. 2000; 25 153-159
- 15 Fang J, Dagenais S L, Erickson R P et al.. Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome. Am J Hum Genet. 2000; 67 1382-1388
- 16 Heimpel H, Bierich J R, Herrmann J M, Meister H, Vollmar J. Dysplasia of the lymphatics with lymphoedema, generalized lympangiectasis, chylothorax and “pseudo-storage-disease”. Lymphology. 1979; 12 228-240
Masayuki OchiaiM.D.
Department of Pediatrics, Graduate School of Medical Sciences
Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582, Japan