Kikuchi disease

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Kikuchi-Fujimoto disease
Histiocytic necrotizing lymphadenitis - intermed mag.jpg
Micrograph of a lymph node with Kikuchi disease showing the characteristic features (abundant histiocytes, necrosis without neutrophils). H&E stain.
Classification and external resources
Specialty Lua error in Module:Wikidata at line 446: attempt to index field 'wikibase' (a nil value).
eMedicine med/3663
Patient UK Kikuchi disease
MeSH D020042
[[[d:Lua error in Module:Wikidata at line 863: attempt to index field 'wikibase' (a nil value).|edit on Wikidata]]]

Kikuchi-Fujimoto disease (KFD) was described in 1972 in Japan. It is also known as Kikuchi disease, histiocytic necrotizing lymphadenitis, Kikuchi necrotizing lymphadenitis, phagocytic necrotizing lymphadenitis, subacute necrotizing lymphadenitis, and necrotizing lymphadenitis.[1][2][3][4]

It was first described in Japan by Dr Masahiro Kikuchi in 1972[5] and independently by Y. Fujimoto.

Epidemiology

Kikuchi-Fujimoto disease (KFD) is a rare, self-limiting disorder that typically affects the cervical lymph nodes. Recognition of this condition is crucial, especially because it can easily be mistaken for tuberculosis, lymphoma, or even adenocarcinoma. Awareness of this disorder will help prevent misdiagnosis and inappropriate treatment.[1]

Kikuchi's disease is a very rare disease and mainly seen in Japan. Isolated cases are reported in America, Europe and Asia. It is mainly a disease of young adults (mean age, 20–30 years), with a slight bias towards females. The cause of this disease is not known although infectious and autoimmune etiologies have been proposed. Course of the disease is generally benign and self-limiting. Lymphadenopathy most often resolves over several weeks to six months. Recurrence rate is about 3%. Mortality is extremely rare and usually due to hepatic, respiratory, or cardiac failure.

Pathophysiology

Some studies have suggested a genetic predisposition to the proposed autoimmune response. Several infectious candidates have been associated with Kikuchi's disease.[6]

There are many postulates about the etiology of KFD. A microbial/viral or autoimmune cause has been suggested. Mycobacterium szulgai, Yersinia and Toxoplasma have been implicated. More recently there has been growing evidence of the role of Epstein-Barr virus, as well as other viruses (HHV6, HHV8, Parvovirus B19, HIV- and HTLV-1) in the pathogenesis of KFD.[1] However, many independent studies have failed to identify the presence of these infectious agents in cases of Kikuchi lymphadenopathy.[7] In addition, serologic tests including antibodies to a host of viruses have consistently proven noncontributory and no viral particles have been identified ultrastructurally. It is now proposed that KFD is a nonspecific hyperimmune reaction to a variety of infectious, chemical, physical and neoplastic agents. In addition to SLE, other autoimmune conditions and manifestations such as antiphospholipid syndrome, polymyositis, systemic juvenile idiopathic arthritis, bilateral uveitis, arthritis and cutaneous necrotizing vasculitis have been linked to KFD. It is possible that KFD may represent an exuberant T-cell mediated immune response in a genetically susceptible individual to a variety of non-specific stimuli.[1]

Human leukocyte antigen class II genes are more frequent in patients with Kikuchi disease, suggesting a genetic predisposition to the proposed autoimmune response.

Clinical Features

The signs and symptoms of Kikuchi's disease are fever, lymphadenopathy, skin rashes and headache. Rarely hepatosplenomegaly and nervous system involvement resembling meningitis is seen. Differential diagnosis includes SLE, disseminated tuberculosis, lymphoma, Sarcoidosis, and viral lymphadenitis.Clinical findings sometimes may include positive results for IgM/IgG/IgA Antibodies.

For other causes of lymph node enlargement, see lymphadenopathy.

Diagnosis

It is diagnosed by lymph node excision biopsy.

Kikuchi's disease is a self-limiting illness which has symptoms which may overlap with Hodgkin's lymphoma leading to misdiagnosis in some patients.

ANA, APLA, Anti-dsDNA, RF are usually negative, and may help in differentiating from SLE.

Management

No specific cure. Treatment largely supportive. NSAIDs for tender lymph nodes and fever, corticosteroids are useful in severe extranodal or generalized disease.

Symptomatic measures aimed at relieving the distressing local and systemic complaints have been described as the main line of management of KFD. Analgesics, antipyretics, nonsteroidal anti-inflammatory drugs(NSAIDs) and corticosteroids have been used. If the clinical course is more severe, with multiple flares of bulky cervical lymphadenopathy and fever, then a low-dose corticosteroid treatment has been suggested.

See also

References

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  5. Kikuchi M. Lymphadenitis showing focal reticulum cell hyperplasia with nuclear debris and phagocytes. Acta Hematol Jpn 1972;35:379–80.
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