Rossolimo-Melkerson-Rosental syndrome
Last reviewed: 23.04.2024
All iLive content is medically reviewed or fact checked to ensure as much factual accuracy as possible.
We have strict sourcing guidelines and only link to reputable media sites, academic research institutions and, whenever possible, medically peer reviewed studies. Note that the numbers in parentheses ([1], [2], etc.) are clickable links to these studies.
If you feel that any of our content is inaccurate, out-of-date, or otherwise questionable, please select it and press Ctrl + Enter.
Rossolimo-Melkerson-Rosenthal syndrome is a chronically relapsing dermatosis of unclear etiology.
In its development, importance is attached to genetic factors, functional disorders of the nervous system such as angioneurosis, infectious and allergic mechanisms. It is manifested by a combination of granulomatous cheilitis (less infiltration and swelling of other parts of the face), paresis (or paralysis) of the facial nerve and folded tongue.
Pathomorphology of the Rossolimo-Melkerson-Rosenthal syndrome. In some cases, the picture is non-specific, tissue edema is observed, in others granulomatous changes are observed, identical with those in sarcoidosis or granulomatous cheilate of Misher, sometimes against a background of nonspecific lymphocytic infiltration, perivascular as well as peri-follicular granulomas are visible.
What do need to examine?
How to examine?