Literature DB >> 23853197

Relapsing fevers and lymphadenopathy in a young woman.

Raghuwansh P Sah1, Michael E Wilson, Justin Seningen, Anjali Bhagra.   

Abstract

A 23-year-old woman presented to the emergency department with severe occipital headache, nausea and fever. She was treated with intravenous antibiotics for suspected meningitis. After a brief period of response, her symptoms relapsed and remained refractory despite continuing intravenous antibiotics for 10 days leading to referral to our centre. Physical examination was significant for tender right cervical lymph node. Initial tests included pancytopenia, elevated C reactive protein, lactate dehydrogenase and unremarkable cerebrospinal fluid. Extensive infectious and rheumatology work-up was negative. Massive posterior cervical, axillary and inguinal lymphadenopathy was revealed on imaging. Excisional biopsy of the deep cervical lymph node showed histiocytic necrotising lymphadenitis suggesting a diagnosis of Kikuchi disease. Her course was complicated by acute renal failure. Her symptoms resolved in about a week with supportive treatment along with improvement in pancytopenia and renal function. She had two additional self-limited recurrences in the next 3 months and remains symptom free thereafter.

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Year:  2013        PMID: 23853197      PMCID: PMC3736281          DOI: 10.1136/bcr-2013-200237

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  13 in total

1.  Histiocytic necrotizing lymphadenitis in the context of systemic lupus erythematosus (SLE): Is histiocytic necrotizing lymphadenitis in SLE associated with skin lesions?

Authors:  S K Kim; M S Kang; B Y Yoon; D Y Kim; S K Cho; S C Bae; M Y Her
Journal:  Lupus       Date:  2011-05-11       Impact factor: 2.911

2.  Histiocytic necrotizing lymphadenitis (Kikuchi-Fujimoto's disease) mimicking systemic lupus erythematosus: a review of two cases.

Authors:  M Yilmaz; C Camci; I Sari; V Okan; A Sevinc; A M Onat; H Buyukhatipoglu
Journal:  Lupus       Date:  2006       Impact factor: 2.911

3.  The histopathology of cutaneous lesions of Kikuchi's disease (necrotizing lymphadenitis): a report of five cases.

Authors:  J Spies; K Foucar; C T Thompson; P E LeBoit
Journal:  Am J Surg Pathol       Date:  1999-09       Impact factor: 6.394

Review 4.  Histiocytic necrotizing lymphadenitis (Kikuchi's disease) with aseptic meningitis.

Authors:  Y Sato; H Kuno; K Oizumi
Journal:  J Neurol Sci       Date:  1999-03-01       Impact factor: 3.181

5.  Kikuchi's histiocytic necrotizing lymphadenitis: an analysis of 108 cases with emphasis on differential diagnosis.

Authors:  R F Dorfman; G J Berry
Journal:  Semin Diagn Pathol       Date:  1988-11       Impact factor: 3.464

6.  Kikuchi's disease (histiocytic necrotizing lymphadenitis). A clinicopathologic study of 79 cases with an analysis of histologic subtypes, immunohistology, and DNA ploidy.

Authors:  T T Kuo
Journal:  Am J Surg Pathol       Date:  1995-07       Impact factor: 6.394

7.  Kikuchi's lymphadenitis. A morphologic analysis of 75 cases with special reference to unusual features.

Authors:  W Y Tsang; J K Chan; C S Ng
Journal:  Am J Surg Pathol       Date:  1994-03       Impact factor: 6.394

8.  Kikuchi-Fujimoto Disease: analysis of 244 cases.

Authors:  Yasar Kucukardali; Emrullah Solmazgul; Erdogan Kunter; Oral Oncul; Sukru Yildirim; Mustafa Kaplan
Journal:  Clin Rheumatol       Date:  2006-03-15       Impact factor: 3.650

Review 9.  Kikuchi-Fujimoto disease.

Authors:  Xavier Bosch; Antonio Guilabert
Journal:  Orphanet J Rare Dis       Date:  2006-05-23       Impact factor: 4.123

10.  Kikuchi's disease: a review and analysis of 61 cases.

Authors:  Hsin-Ching Lin; Chih-Ying Su; Chao-Cheng Huang; Chung-Feng Hwang; Chih-Yen Chien
Journal:  Otolaryngol Head Neck Surg       Date:  2003-05       Impact factor: 5.591

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  1 in total

1.  Rosai-Dorfman disease affecting the nasal cavities and paranasal sinuses.

Authors:  Bruno Niemeyer de Freitas Ribeiro; Edson Marchiori
Journal:  Radiol Bras       Date:  2016 Jul-Aug
  1 in total

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