2018, Number 2
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Med Int Mex 2018; 34 (2)
Kikuchi-Fujimoto disease in presentation with silicosis
Bolaños-Aguilar MA, Celis-Vera KD, Barragán-Garfias JA, Orrantia-Vértiz M, Duarte-Mote J
Language: Spanish
References: 23
Page: 335-341
PDF size: 385.65 Kb.
ABSTRACT
Kikuchi-Fujimoto disease, also called histiocytic necrotizing lymphadenitis,
is a rare and benign condition of unknown etiology, characte
rized by cervical lymphadenopathy with fever that frequently occurs
in previously young healthy women. The clinical manifestations, a
history of systemic lupus erythematous and histopathologic analysis
suggest an immune response of T cells and histiocytes as a part of the
pathophysiology. The diagnosis of Kikuchi disease requires lymph
node biopsy, in which there is evidence of necrosis with histiocyte
infiltrates and characteristically absence of neutrophils. No effective
treatment exists for Kikuchi disease, it is self-limited into 1-4 weeks;
with severe and persistent symptoms, glucocorticoids and nonsteroidal
anti-inflammatory drugs are prescribed. Silicosis is a condition in
which silicone, a component of breast implants, acts as an immunogenic
adjuvant, causing a local and systemic autoimmune response
with non-specific symptomatology constituting the adjuvant-induced
autoimmune syndrome (ASIA). The treatment of ASIA is based on the
elimination of the external stimulus and in most cases a favorable
long-term response is observed without initiating immunomodulatory
treatment. More cases are needed in order to establish silicosis
as a cause of Kikuchi-Fujimoto disease and to know more about the
relationship between these conditions.
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