Ultrastructural aspects of the thyroid in a case of human congenital goitre with cretinism

Ketelbant-Balasse, P.; Glinoer, D.; Neve, P.

Pathologia Europaea 10(2): 155-165

1975


ISSN/ISBN: 0031-2967
PMID: 171610
Document Number: 83230
Transmission and scanning electron microscope studies in a case of congenital goiter associated with cretinism revealed the existence of 2 cell types: the 1st with rounded endoplasmic cisternae and normal lysosomes; the 2nd characterized by an abundance of lysosomes and/or lipofuscin granules. Intermediary aspects suggested that the 2nd cell type was the progeny of the 1st type. As colloid droplets and apical pseudopods engulfing colloid were nearly absent, and as non-butanol extractable 127I was elevated in the plasma, it is suggested that iodoprotein secretion occurred by a process different from colloid phagocytosis as observed after acute thyrotropin stimulation.

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