Pregled bibliografske jedinice broj: 870937
Life-threatening onset of systemic lupus erythematosus coincides with Kikuchi disease in a Croatian patient : Case reports
Life-threatening onset of systemic lupus erythematosus coincides with Kikuchi disease in a Croatian patient : Case reports // The Egyptian rheumatologist, 39 (2017), 4; 259-261 doi:10.1016/j.ejr.2017.04.003 (međunarodna recenzija, članak, stručni)
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Naslov
Life-threatening onset of systemic lupus erythematosus coincides with Kikuchi disease in a Croatian patient : Case reports
Autori
Holik, Hrvoje ; Kovač Peić, Anamarija ; Coha, Božena
Izvornik
The Egyptian rheumatologist (1110-1164) 39
(2017), 4;
259-261
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, stručni
Ključne riječi
Kikuchi disease ; Systemic lupus erythematosus
Sažetak
Kikuchi disease (KD) or histiocytic necrotizing lymphadenitis is a benign self-limited extremely- rare disorder of unkown etiology. It is characterized by regional cervical lymphadenopathy with tenderness, usually accompanied with mild fever and night sweats. The recognition of KD is crucial as it can be mistaken for or be associated with systemic lupus erythematosus (SLE). Case report We present a 29-year-old Croatian female admitted to the Hematology and Oncology Department, General Hospital Dr. Josip Benčević, Croatia in a life threatening condition. She was feverish (40 °C) with chills and weight loss. On clinical examination the patient had bilaterally enlarged cervical, axillary and inguinal lymph nodes with sizes up to 3 cm. Our differential diagnosis was SLE, lymphoma, sarcoidosis, Still’s disease, hemophagocytic syndrome and KD. An extensive workup was done to confirm one of these diagnoses. Methylprednisolone 100 mg iv (1.5 mg/kg) was initiated for 5 days and as the patient’s condition was severe, steroids were maintained. Lymph node biopsy histopathology was compatible with KD. Antinuclear antibody and anti- double- stranded-DNA were positive. The patient fulfilled the classification criteria for SLE. A diagnosis of SLE associated with KD was held. On CT scan there was bilateral pleural effusion and ascites. Brain MRI was compatable with lupus cerebritis. On steroids plus hydroxychloroquine the patient remarkably improved and remained in remission after 3 months. Prompt diagnosis and treatment with steroids may save the life of SLE patients with KD and leads to a favorable outcome. Raising the awareness towards this possibly serious association is important.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Ustanove:
Opća bolnica "Dr. Josip Benčević"
Citiraj ovu publikaciju:
Časopis indeksira:
- Web of Science Core Collection (WoSCC)
- Emerging Sources Citation Index (ESCI)
- Scopus