Pregled bibliografske jedinice broj: 597922
Kikuchi-Fujimoto Disease: Early Diagnosis with FNAC
Kikuchi-Fujimoto Disease: Early Diagnosis with FNAC // Cytopathology, 23 (Suppl 1) / Herbert, A ; Cochand-Priollet, B (ur.).
Oxford: Wiley-Blackwell, 2012. str. 80-80 (ostalo, međunarodna recenzija, sažetak, stručni)
CROSBI ID: 597922 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Kikuchi-Fujimoto Disease: Early Diagnosis with FNAC
Autori
Podrug, Ljiljana ; Kaić, Gordana ; Jelić Puškarić, Biljana ; Šiftar, Zoran ; Benić, Branka ; Vladušić Lučić, I ; Kardum-Skelin, Ika.
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, stručni
Izvornik
Cytopathology, 23 (Suppl 1)
/ Herbert, A ; Cochand-Priollet, B - Oxford : Wiley-Blackwell, 2012, 80-80
Skup
37th European Congress of Cytology
Mjesto i datum
Cavtat, Hrvatska; Dubrovnik, Hrvatska, 30.09.2012. - 03.10.2012
Vrsta sudjelovanja
Ostalo
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
FNAC; Kikuchi-Fujimoto disease
Sažetak
Background: Kikuchi-Fujimoto disease (KFD) or histiocytic necrotizing lymphadenitis is very rare, benign enlargment of the lymph nodes. It usually present with fever, lymphadenopathy, skin rash and headache. The KFD has benign and self-limiting course. The accurate diagnosis of KFD on fine-needle aspiration cytology (FNAC) is possible on adequately sampled and well prepared specimen complemented with full and accurate clinical data. Case: An 18-year old female presented with painful, progressive enlargement of subangular lymph nodes, fever (up 39.7 C), headache, sore throat and skin rash (above elbow and knee). On admission the patient was febrile (38.9 C) with 2.2 cm and 1.5 cm large, left subangilar, hard, movable and painfull lymph nodes. Laboratory studies revealed only elevated erythrocyte sedimentation rate and C-reactive protein. FNAC of lymph nodes showed karyorrhectic and granular debris, crescentic histiocytes and plasmacytoid monocytes on reactive lymphoid background. Imunocytochemically, crescentic histiocytes were expressed MPO and CD68, plasmacytoid monocytes were positive for CD68, but not for MPO. Cytological and immunocytochemical findings confirmed definitive diagnosis of KFD. Lymph node flow cytometry showed polyclonal lymphocyte population. Additional serologic test for parvovirus B19 was positive, while test for EBV, CMV, toxoplasmosis and adenovirus were negative. Several weeks later the patient is well without any signs of local and systemic disease. Conclusion: Differential diagnosis of KFD includes lymphoma, TBC lymphadenitis and lupus lymphadenopathy. An early FNAC diagnostic prevents unnecessary procedures and potentially harmful treatments.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Projekti:
108-1081873-1893 - Prognostički faktori, dijagnostika i terapija hemoblastoza (Jakšić, Branimir, MZOS ) ( CroRIS)
198-1980955-0953 - Imunobiologija kronične B-limfocitne leukemije i mikrookoliš (Jakšić, Ozren, MZOS ) ( CroRIS)
Ustanove:
Klinička bolnica "Merkur",
Medicinski fakultet, Zagreb,
Klinika za infektivne bolesti "Dr Fran Mihaljević",
Akademija medicinskih znanosti
Profili:
Ika Kardum-Skelin
(autor)
Zoran Šiftar
(autor)
Gordana Kaić
(autor)
Branka Benić
(autor)
Biljana Jelić Puškarić
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE