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  1. Article ; Online: A Rare Neurological Presentation of Kikuchi-Fujimoto Disease.

    Asad, Murva / Mehta, Arpan R / Mallon, Dermot

    JAMA neurology

    2024  

    Language English
    Publishing date 2024-04-15
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2702023-X
    ISSN 2168-6157 ; 2168-6149
    ISSN (online) 2168-6157
    ISSN 2168-6149
    DOI 10.1001/jamaneurol.2024.0799
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    Ui II Zs.191: Show issues Location:
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  2. Article ; Online: Kikuchi-Fujimoto disease during early pregnancy.

    Ichikawa, Go / Negishi, Yasuyuki / Chishima, Fumihisa / Suzuki, Shunji

    The journal of obstetrics and gynaecology research

    2024  

    Abstract: Kikuchi-Fujimoto disease (KFD) is rare during pregnancy. It is characterized by necrotizing ...

    Abstract Kikuchi-Fujimoto disease (KFD) is rare during pregnancy. It is characterized by necrotizing lymphadenitis and often occurs in young Asian women. We report a case of KFD during pregnancy, which was difficult to diagnose. A 37-year-old pregnant female (gestational week [GW] 7
    Language English
    Publishing date 2024-03-21
    Publishing country Australia
    Document type Case Reports
    ZDB-ID 1327307-3
    ISSN 1447-0756 ; 1341-8076
    ISSN (online) 1447-0756
    ISSN 1341-8076
    DOI 10.1111/jog.15928
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    Zs.A 1810: Show issues Location:
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  3. Article ; Online: Pulmonary Involvement of Kikuchi-Fujimoto Disease in Rheumatoid Arthritis.

    Huang, Hao-Yu / Ko, Kai-Hsiung

    Journal of clinical rheumatology : practical reports on rheumatic & musculoskeletal diseases

    2024  Volume 30, Issue 4, Page(s) e122

    MeSH term(s) Humans ; Histiocytic Necrotizing Lymphadenitis/diagnosis ; Histiocytic Necrotizing Lymphadenitis/complications ; Arthritis, Rheumatoid/complications ; Arthritis, Rheumatoid/diagnosis ; Female ; Tomography, X-Ray Computed/methods ; Middle Aged ; Treatment Outcome ; Lung/diagnostic imaging ; Male ; Diagnosis, Differential
    Language English
    Publishing date 2024-03-20
    Publishing country United States
    Document type Case Reports ; Journal Article
    ZDB-ID 1283266-2
    ISSN 1536-7355 ; 1076-1608
    ISSN (online) 1536-7355
    ISSN 1076-1608
    DOI 10.1097/RHU.0000000000002077
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    Zs.A 4815: Show issues Location:
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  4. Article: Kikuchi-Fujimoto disease: A comprehensive review.

    Mahajan, Vikram K / Sharma, Vikas / Sharma, Neeraj / Rani, Ritu

    World journal of clinical cases

    2023  Volume 11, Issue 16, Page(s) 3664–3679

    Abstract: Kikuchi-Fujimoto disease, a rare form of necrotizing lymphadenitis, is an uncommon, benign, self ... Both Kikuchi-Fujimoto disease and systemic lupus erythematosus share an obscure and complex relationship as systemic ... with Kikuchi-Fujimoto disease. It is often mistaken for non-Hodgkin lymphoma while lupus lymphadenitis, cat-scratch disease ...

    Abstract Kikuchi-Fujimoto disease, a rare form of necrotizing lymphadenitis, is an uncommon, benign, self-limiting disorder of obscure etiology. It affects mostly young adults of both genders. Clinically, it presents with fever and lymphadenopathy of a firm to rubbery consistency frequently involving cervical lymph nodes while weight loss, splenomegaly, leucopenia, and elevated erythrocyte sedimentation rate feature in severely affected patients. Cutaneous involvement occurs in about 30%-40% of cases as facial erythema and nonspecific erythematous papules, plaques, acneiform or morbilliform lesions of great histologic heterogeneity. Both Kikuchi-Fujimoto disease and systemic lupus erythematosus share an obscure and complex relationship as systemic lupus erythematosus may occasionally precede, develop subsequently, or sometimes be associated concurrently with Kikuchi-Fujimoto disease. It is often mistaken for non-Hodgkin lymphoma while lupus lymphadenitis, cat-scratch disease, Sweet's syndrome, Still's disease, drug eruptions, infectious mononucleosis, and viral or tubercular lymphadenitis are other common differentials. Fine needle aspiration cytology mostly has features of nonspecific reactive lymphadenitis and immunohistochemistry studies usually show variable features of uncertain diagnostic value
    Language English
    Publishing date 2023-06-13
    Publishing country United States
    Document type Journal Article ; Review
    ISSN 2307-8960
    ISSN 2307-8960
    DOI 10.12998/wjcc.v11.i16.3664
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: A Rare Case of Kikuchi-Fujimoto Disease.

    Qasim, Abeer / Itare, Vikram / Anwar, Muhammad Yasir / Arguello Perez, Esther

    Cureus

    2023  Volume 15, Issue 5, Page(s) e39098

    Abstract: Kikuchi-Fujimoto disease (KFD) is an autoimmune condition that is more common in females and occurs ... cervical lymphadenopathy, night sweats, myalgia, and rashes. The disease can be misdiagnosed as reactive ... for the disease, usually symptomatic and supportive measures are effective; however, steroids and ...

    Abstract Kikuchi-Fujimoto disease (KFD) is an autoimmune condition that is more common in females and occurs in the third decade of life. The condition is usually benign and self-resolving and is characterized by fever, cervical lymphadenopathy, night sweats, myalgia, and rashes. The disease can be misdiagnosed as reactive follicular hyperplasia, tuberculous lymphadenitis, systemic lupus erythematosus, and malignant lymphoma. The diagnosis of KFD involves the excision of the affected lymph node. Although there is no specific treatment for the disease, usually symptomatic and supportive measures are effective; however, steroids and immunosuppressive therapies are considered in more severe cases. The disease lasts for around one to four months. The neurological complications include cerebellar ataxia, meningoencephalitis, and aseptic meningitis. Here, we describe the case of a 36-year-old male who presented with complaints of fever, malaise chills, anorexia, and fatigue associated with a tender right axillary lymph node. The patient underwent a biopsy which confirmed KFD and responded well to supportive therapy.
    Language English
    Publishing date 2023-05-16
    Publishing country United States
    Document type Case Reports
    ZDB-ID 2747273-5
    ISSN 2168-8184
    ISSN 2168-8184
    DOI 10.7759/cureus.39098
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Conference proceedings: A case of Kikuchi-Fujimoto Disease

    Hellwig, Maria Isabel / Gonzalez, Mireia Donate / Stuhlmann-Laeisz, Maria Christiane

    Laryngo-Rhino-Otologie

    2023  Volume 102, Issue S 02

    Event/congress 94th Annual Meeting German Society of Oto-Rhino-Laryngology, Head and Neck Surgery e.V., Bonn, Congress Center Leipzig, 2023-05-17
    Language English
    Publishing date 2023-05-01
    Publisher Georg Thieme Verlag
    Publishing place Stuttgart ; New York
    Document type Article ; Conference proceedings
    ZDB-ID 96005-6
    ISSN 1438-8685 ; 0935-8943 ; 0340-1588
    ISSN (online) 1438-8685
    ISSN 0935-8943 ; 0340-1588
    DOI 10.1055/s-0043-1767114
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    Ul II Zs.95: Show issues Location:
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  7. Article ; Online: Anaemic retinopathy in Kikuchi-Fujimoto disease.

    Vaidya, Harshit

    Indian journal of ophthalmology

    2022  Volume 70, Issue 7, Page(s) 2715–2716

    MeSH term(s) Anemia ; Diagnosis, Differential ; Histiocytic Necrotizing Lymphadenitis/complications ; Histiocytic Necrotizing Lymphadenitis/diagnosis ; Humans ; Retinal Diseases/diagnosis ; Retinal Diseases/etiology
    Language English
    Publishing date 2022-07-05
    Publishing country India
    Document type Journal Article
    ZDB-ID 187392-1
    ISSN 1998-3689 ; 0301-4738
    ISSN (online) 1998-3689
    ISSN 0301-4738
    DOI 10.4103/ijo.IJO_2632_21
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    Zs.B 329: Show issues Location:
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  8. Article: Kikuchi-Fujimoto Disease: A Rare Presentation in a Young Male.

    Kedar, Aishwarya K / Ghewade, Babaji / Jadhav, Ulhas / Wagh, Pankaj / Alone, Vivek D

    Cureus

    2024  Volume 16, Issue 3, Page(s) e55615

    Abstract: Kikuchi-Fujimoto disease (KFD), also known as histiocytic necrotizing lymphadenitis, is a rare ...

    Abstract Kikuchi-Fujimoto disease (KFD), also known as histiocytic necrotizing lymphadenitis, is a rare benign condition characterized by cervical lymphadenopathy and constitutional symptoms mimicking tuberculosis. We present the case of a 22-year-old male who presented with fever, dry cough, loss of appetite, multiple joint pains for 15 days, and loss of weight for one month. Physical examination revealed palpable cervical, occipital, axillary, and inguinal lymphadenopathy, and laboratory investigations were within normal limits except for raised erythrocyte sedimentation rate (ESR). Contrast-enhanced computed tomography (CECT) showed mediastinal lymphadenopathy with no pleuroparenchymal abnormality of the lung. Excision biopsy of a cervical lymph node confirmed necrotizing lymphadenitis consistent with KFD. The patient was treated with nonsteroidal anti-inflammatory drugs (NSAIDs) and glucocorticoids, resulting in the resolution of symptoms and regression of lymphadenopathy. This case signifies the importance of considering KFD in the differential diagnosis of lymphadenopathy and highlights the significance of histopathological evaluation for accurate diagnosis and management guidance.
    Language English
    Publishing date 2024-03-06
    Publishing country United States
    Document type Case Reports
    ZDB-ID 2747273-5
    ISSN 2168-8184
    ISSN 2168-8184
    DOI 10.7759/cureus.55615
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Correction to 'Immunopathology of Kikuchi-Fujimoto disease: A reappraisal using novel immunohistochemistry markers'.

    Histopathology

    2024  Volume 84, Issue 4, Page(s) 719

    Language English
    Publishing date 2024-01-16
    Publishing country England
    Document type Published Erratum
    ZDB-ID 131914-0
    ISSN 1365-2559 ; 0309-0167
    ISSN (online) 1365-2559
    ISSN 0309-0167
    DOI 10.1111/his.15132
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    Zs.A 1328: Show issues Location:
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  10. Article ; Online: Disappearing choroidal mass: Ophthalmic manifestations of a Presumed Kikuchi-Fujimoto disease.

    Rodríguez-Castro, Selene / Fromow-Guerra, Jans / Garza-González, Salvador / Pinilla-Monroy, Angela / Soberon, Vidal

    Retinal cases & brief reports

    2024  

    Abstract: Purpose: to report our findings in a patient with presumed Kikuchi-Fujimoto disease.: Methods ... patient who presented with an unusual form of symptoms that fit a disease called Kikuchi-Fujimoto disease ... gone.: Conclusion: large choroidal masses can occur in patients with Kikuchi-Fujimoto disease ...

    Abstract Purpose: to report our findings in a patient with presumed Kikuchi-Fujimoto disease.
    Methods: report of clinical findings, fundus images, OCT, and ultrasonography.
    Results: a 19-year-old female patient who presented with an unusual form of symptoms that fit a disease called Kikuchi-Fujimoto disease (KFD). A large choroidal mass was observed in the posterior pole, a month later the mass was completely gone.
    Conclusion: large choroidal masses can occur in patients with Kikuchi-Fujimoto disease, these do not warrant treatment as they are self-limiting.
    Language English
    Publishing date 2024-01-12
    Publishing country United States
    Document type Journal Article
    ISSN 1937-1578
    ISSN (online) 1937-1578
    DOI 10.1097/ICB.0000000000001544
    Database MEDical Literature Analysis and Retrieval System OnLINE

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