In this article, we will address the topic of Riga–Fede disease from a broad and multidisciplinary perspective. Riga–Fede disease is a topic of great relevance today, which has captured the attention of specialists and the general public. Throughout history, Riga–Fede disease has played a fundamental role in various aspects of society, culture and everyday life. Through this article, we will explore the various approaches, debates and perspectives that revolve around Riga–Fede disease, with the aim of offering a comprehensive and enriching vision on this topic.
Riga–Fede disease | |
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Riga-Fede disease on the lower lip. |
Riga–Fede disease (RFD) is a rare and benign mucosal condition,[1] characterized by a tongue ulcer that is frequently brought on by traumatizing injuries sustained from repeatedly moving the tongue back and forth over the mandibular anterior incisors.[2]
Clinically, it typically manifests as a tongue-localized ulcer (60 percent of lesions), though it can also affect the lip, palate, gingiva, vestibular mucosa, and floor of the mouth. RFD may not cause any symptoms or may occasionally be accompanied by pain.[3]
RFD is most frequently linked to the emergence of the natal-neonatal teeth in newborns[4] or the primary lower incisor in older infants.[5]
Histopathologically speaking, RFD is characterized by mucosal areas that are ulcerated, granulation tissue present, and a mixed inflammatory infiltrate that is abundant in mast cells, macrophages, lymphocytes, and eosinophils.[6]
The lesion can be removed, the sharp incisal edges can be smoothed, or the tooth's sharp edges can be rounded with composite increments. The latter is where mild to moderate ulceration can occur. Teeth extraction may be helpful if the ulceration is large and preventing the patient from eating.[7]