- Author:
Weon Seo PARK
1
;
Je G CHI
Author Information
- Publication Type:Case Reports
- Keywords: Neuroblastoma; Neuroblastoma in situ; Microcephaly
- MeSH: Adrenal Gland Neoplasms/complications/*congenital/pathology; Adult; Carcinoma in Situ/complications/*congenital/pathology; Female; Humans; Infant, Newborn; *Microcephaly/complications/pathology; Neuroblastoma/complications/*congenital/pathology; Pregnancy
- From:Journal of Korean Medical Science 1993;8(2):99-103
- CountryRepublic of Korea
- Language:English
- Abstract: We present an autopsy case of a two-day-old female infant with a very unusual combination of neuroblastoma in situ in both adrenals and microcephaly. This baby was born to a 28-year-old mother after 38 weeks of gestation, and died of respiratory difficulty 2 days later. At autopsy, the baby weighted 1,840gm, and the brain was extraordinarily small with a weight of 125gm. The gyral pattern was simplified and irregular. Microscopically massive migration defects, pachygyria, micropolygyria, leptomeningeal glioneuronal islands, small corticospinal tract and heterotopic Purkinje cells in the cerebellum were found. In addition, there were medullary nodules in both adrenals. They measured 0.7 x 0.4cm and 0.7 x 0.3cm, respectively. These nodules showed the typical histological features of undifferentiated neuroblastoma. The tumor nodules were confined to the medullary portion and did not extend to the cortex or contiguous structures meeting the criteria of neuroblastoma in situ. Based on these unusual and seemingly unrelated sets of findings, it is suggested that the histogenesis of neuroblastoma in situ could be a part of the generalized dysontogenic process.