Articulo de referencia

Paraganglion

A paraganglion (pl. paraganglia) is a group of non- neuronal cells derived of the neural crest . They are named for being generally in close proximity to sympathetic ganglia . T...

A paraganglion (pl. paraganglia) is a group of non-neuronal cells derived of the neural crest. They are named for being generally in close proximity to sympathetic ganglia. They are essentially of two types: (1) chromaffin or sympathetic paraganglia made of chromaffin cells and (2) nonchromaffin or parasympathetic paraganglia made of glomus cells. They are neuroendocrine cells, the former with primary endocrine functions and the latter with primary chemoreceptor functions.[1]

Chromaffin paraganglia (also called chromaffin bodies) are connected with the ganglia of the sympathetic trunk and the ganglia of the celiac, renal, adrenal, aortic and hypogastric plexuses. They are concentrated near the adrenal glands and essentially function the same way as the adrenal medulla. They are sometimes found in connection with the ganglia of other sympathetic plexuses. None have been found with the sympathetic ganglia associated with the branches of the trigeminal nerve. The largest chromaffin paraganglion is the organ of Zuckerkandl, it is probably the largest source of circulating catecholamines in the fetus and young infants, and gradually atrophies to microscopic loci.[1]

Nonchromaffin paraganglia include carotid bodies and aortic bodies, some are distributed in the ear, along the vagus nerve, in the larynx and at various other places.[2]

Clinical significance

Tumors of the paraganglionic tissues are known as paragangliomas, though this term tends to imply the nonchromaffin type, and can occur at a number of sites throughout the body.

Chromaffin paragangliomas are issued from chromaffin cells, and are known as pheochromocytomas. Adrenal pheochromocytomas are usually benign while extra-adrenal ones are more malignant.[3] They are most of the time in the adrenals, and only rarely outside of the abdomen. They usually secrete hormones and estimates of a familial history vary.[1][2]

Los paragangliomas no cromafines suelen ser benignos. [ 3 ] Generalmente se presentan en la cabeza y el cuello, con mayor frecuencia en el cuerpo carotídeo o yugulotimpánico, rara vez secretan hormonas y suelen tener antecedentes familiares. [ 1 ] [ 2 ]

Referencias

Dominio públicoEste artículo incorpora texto de dominio público de la página 1277 de  la vigésima edición de Gray's Anatomy (1918).

  1. 1 2 3 4 Anne Marie McNicol (2010). "Capítulo 12: Médula suprarrenal y paraganglios". Patología endocrina: diagnóstico diferencial y avances moleculares (ed. Springer  ). pág.  281.
  2. 1 2 3 Clasificación de tumores de la OMS (2005). «Tumores del sistema paraganglionar». Patología y genética de los tumores de cabeza y cuello (PDF) . Lyon: IARC Press. ISBN 9283224175. Archivado del original (PDF) el 08-08-2014 . Consultado el 01-03-2013 .
  3. ^ Klöppel , G (julio de 2003). "Tumores de la médula suprarrenal y paraganglios]". El patologo . 24 (4): 280– 6. doi : 10.1007/s00292-003-0635-8 . PMID 14513275 . S2CID 33216313 .