Pregled bibliografske jedinice broj: 682104
A case of Melkersson‐Rosenthal syndrome associated with oligodontia in 15 years old girl.
A case of Melkersson‐Rosenthal syndrome associated with oligodontia in 15 years old girl. // Book of abstracts 4th Croatian Congress of Neuroscience
Zagreb: Hrvatsko društvo za neuroznanost ; Hrvatski institut za istraživanje mozga Medicinskog fakulteta Sveučilišta u Zagrebu, 2013. (poster, međunarodna recenzija, sažetak, stručni)
CROSBI ID: 682104 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
A case of Melkersson‐Rosenthal syndrome associated with oligodontia in 15 years old girl.
Autori
Krakar, Goran ; Marn, Borut ; Pustišek, Nives ; Ulamec, Monika ; Gojmerac, Tomislav ; Mejaški Bošnjak, Vlatka
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, stručni
Izvornik
Book of abstracts 4th Croatian Congress of Neuroscience
/ - Zagreb : Hrvatsko društvo za neuroznanost ; Hrvatski institut za istraživanje mozga Medicinskog fakulteta Sveučilišta u Zagrebu, 2013
Skup
4th Croatian Congress of Neuroscience
Mjesto i datum
Zagreb, Hrvatska, 20.09.2013. - 21.09.2013
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
Melkersson-Rosenthal syndrome; oligodontia
Sažetak
Objective: We report a case of Melkersson- Rosenthal syndrome (MRS) associated with oligodontia in 15 years old girl. Background: MRS is a rare neuromucocutaneous disorder of uncertain etiology causing localized edema, inflammation in the face and oral cavity, fissuring of the tongue, and recurrent unilateral or alternating facial palsy. Complete clinical form is uncommon and presentation is usually monosymptomatic or oligosymptomatic. Design/Methods: Our patient is a girl at the age of 15 years with recurrent facial palsy (at the age 6, 8 and two times 15), three times left-sided and once right-sided. Initial symptom was unilateral localized non-painful tongue edema, followed by ipsilateral facial edema after 2-3 days, and subsequent development of facial palsy (grade 5 or 6). She had a mild lateral tongue keratosis, indurated on palpation. Taste sensations showed dysgeusia for sweet and salty. Results: Inflammatory, infectology and immunology tests were normal. Due to insufficient teeth, orthopantomogram was performed and showed oligodontia. Brain MRI showed normal brain and facial nerve path, but revealed right arachnoidal cyst with suspected glossopharyngeus compression, clinicaly asymptomatic. Tongue biopsy showed keratosis, acanthosis, edema and mononuclear infiltrates. She was treated with methylprednisolone and doxycycline, with physical therapy, and recovered completely. Conclusions: There is no standard therapy for this syndrome, etiology is still largely unknown. To our knowledge, this is the first report of MRS associated with oligodontia. The diagnosis of MRS is clinical and should be suspected in recurrent facial palsy.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Projekti:
072-1081870-0025 - Neurorazvojni ishod djece s intrauterinim zastojem rasta i/ili hipoksijom (Mejaški-Bošnjak, Vlatka, MZOS ) ( CroRIS)
Ustanove:
Klinika za dječje bolesti Medicinskog fakulteta,
Zdravstveno veleučilište, Zagreb
Profili:
Tomislav Gojmerac
(autor)
Goran Krakar
(autor)
Monika Ulamec
(autor)
Borut Marn
(autor)
Vlatka Mejaški-Bošnjak
(autor)