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Title: Kikuchi’s disease (KD); mimicking malignant lymphoma: A rare cause of cervical lymphadenopathy.
Authors: Ihsan Ullah, Muhammad Khizar Hayat, Sanaullah Khan, Nazish Khan, Chaand Bibi, Maham Rehman
Journal: The Professional Medical Journal (TPMJ)
Publisher: Independent Medical College, Faisalabad- Pakistan
Country: Pakistan
Year: 2022
Volume: 29
Issue: 3
Language: English
DOI: 10.29309/TPMJ/2022.29.03.6627
Keywords: Lymph nodesBiopsyOtolaryngologyHistiocytic necrotizing lymphadenitisKikuchi Disease
Objective: The aim of this study is to present six cases of cervical lymphadenopathy, diagnosed as Kikuchi’s disease and raise the index of suspicion for this disease. Study Design: Case Series. Setting: Histopathology and Otolaryngology/Head & Neck Surgery Department at Rehman Medical Institute (RMI) Peshawar. Period: July 2016 to March 2021. Material & Methods: Records of patients for cases diagnosed as “histiocytic necrotising lymphadenitis” were retrieved, their corresponding patient files accessed from the archive, and case notes analyzed. Results: In this series, a total of six cases of Kikuchi’s disease are presented. A female predominance is evident from the present data (2:1 female to male ratio). All patients presented with palpable lymph nodes in the neck, predominantly on the left (66.7%). Majority (66.7%) presented with neuralgic pain (on/off). Only one patient did not show weight loss and night sweating, the remaining had all the symptoms. All of the patients recovered spontaneously within 6 months (range 2 to 6 months) with symptomatic treatment for neuralgic pain. Conclusion: Kikuchi’s disease should be kept in the differential diagnosis in young females with persistent neck masses, palpable lymph nodes and suspicious fine needle aspiration cytology (FNAC).
To present six cases of cervical lymphadenopathy diagnosed as Kikuchi's disease and to raise the index of suspicion for this disease.
Case Series study conducted at the Histopathology and Otolaryngology/Head & Neck Surgery Departments at Rehman Medical Institute (RMI) Peshawar from July 2016 to March 2021. Records of patients diagnosed with "histiocytic necrotising lymphadenitis" were retrieved, patient files accessed, and case notes analyzed. Histopathology slides were reviewed and re-confirmed.
graph TD;
A[Retrieve records of 'histiocytic necrotising lymphadenitis'] --> B[Access patient files and analyze case notes];
B --> C[Pathologist re-confirms slides];
C --> D[Collect relevant data from case notes];
D --> E[Present findings and analyze results];
E --> F[Formulate conclusion and discussion];
Kikuchi's disease is an increasingly recognized, self-limiting cervical lymphadenitis of unknown origin, predominantly affecting young women. While the exact cause is unknown, autoimmune and infections are considered. The gold standard for diagnosis is lymph node biopsy. The disease can mimic malignant lymphoma, leading to potential misdiagnosis. It is generally benign and self-limiting, with symptomatic treatment being the mainstay.
Six cases of Kikuchi's disease were presented, with a female predominance (2:1 ratio). All patients had palpable neck lymph nodes, predominantly on the left (66.7%). A majority (66.7%) experienced neuralgic pain. All but one patient had weight loss and night sweating. All patients recovered spontaneously within 6 months with symptomatic treatment for pain.
Kikuchi's disease should be considered in the differential diagnosis for young females presenting with persistent neck masses, palpable lymph nodes, and suspicious fine needle aspiration cytology (FNAC). Excision biopsy is crucial for confirmation and to rule out lymphoma. Symptomatic treatment is generally sufficient for this benign condition.
1. Kikuchi's disease was first described in 1972 by Masahiro Kikuchi and Fujimoto. (Confirmed in text)
2. The study presented six cases of Kikuchi's disease. (Confirmed in text)
3. All six patients recovered spontaneously within 6 months with symptomatic treatment for neuralgic pain. (Confirmed in text)
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