Histiocytic Necrotizing Lymphadenitis: A Clinical Study of 6 Children and Review ()
1. Introduction
Histiocytic necrotizing lymphadenitis (HNL), also known as Kikuchi-Fujimoto disease (KFD), is a rare benign and self-limiting disease. This disease was first discovered in Japan in 1972 by Kikuchi and Fujimoto. The etiology and pathogenesis are unknown [1]. According to researches in this field, the possible cause of KFD is considered to be caused by viral infection or autoimmunity [2]. The course of the disease ranges from a few weeks to several months. The main manifestations of HNL are fever, lymphadenopathy (mainly in the neck), leukopenia, and reports of atypical symptoms such as rash, headache, night sweats, weight loss, and nervous system symptoms [3]. HNL is rare in the clinic, and there is no specific clinical manifestations, imaging and laboratory results, so it is easy to be misdiagnosed as upper respiratory tract infection, lymphadenitis, scrofula, malignant lymphoma, infectious mononucleosis and autoimmunity diseases such as systemic lupus erythematosus (SLE). Therefore, we collected the data of children with HNL diagnosed in our hospital and studied in combination with relevant literature to improve our understanding of the disease.
2. Material and Methods
We retrospectively collected the data of 6 pediatric patients with HNL diagnosed by lymph node biopsy from 2012 to 2021 in department of pediatric, the affiliated Changsha Central Hospital, Hengyang Medical School, University of South China, including the clinical characteristics, laboratory examinations, imaging findings and histopathological examinations, treatment and follow-up of the patients and reviewed relevant literatures.
Statistical analyses: continuous variables were presented as mean and 95% CI or median and interquartile range, while categorical variables were described using sample counts and percentages.
3. Results
Among the 6 children, they were not related to each other. The age of onset was from 7 to 14 years old, the median age of onset was 13 years old, the course of illness varied from 1 week to 3 months, and the median time of onset was 10.5 days. Two of the 6 children had a history of cervical lymph node tuberculosis confirmed by lymph node biopsy, and they completed regular and adequate anti-tuberculosis treatment. Four cases had leukopenia, one case had liver damage (increased alanine aminotransferase and aspartate aminotransferase), one case had leukocytosis combined Burkholderia cepacia, three cases had elevated erythrocyte sedimentation rate (ESR) without anemia or thrombocytopenia. All children underwent tuberculosis-related examinations (such as TST, AFB, GeneXpert MTB/RIF, T-SPOT.TB) and those were negative. All children had Epstein-Barr virus serological examination, one was positive and combined with adenovirus infection. Four cases of autoimmune disease tests (such as antinuclear antibodies, rheumatic factors) showed negative, and HIV examinations were all negative. Three cases of bone marrow puncture ruled out blood system diseases. Ultrasound of cervical lymph nodes in all children showed that cervical lymph nodes were enlarged, some of which were combined with enlarged axillary, inguinal or abdominal lymph nodes. All children underwent lymph node biopsy and were diagnosed with HNL, and 5 cases underwent immunohistochemistry (the remaining 1 case was because our hospital had not yet implemented immunohistochemistry technology at the time). (Figure 1: Histologic findings include cortical or paracortical areas presenting varying degrees of coagulative necrosis with abundant karyorrhectic debris, and a large number of different types of histiocytes and immunoblasts surrounding the margin of necrotic areas. Immunophenotypically, a predominance of T cells.) Four children were treated with anti-infective treatment before diagnosis, two children were treated with steroid therapy after diagnosis, including 1 case of oral prednisone and 1 case of intravenous methylprednisolone, and 1 case of weakened immune function was used immunoglobulin for modulating immunity. All the children were improved and discharged, and no recurrence occurred during follow-up. Detailed clinical characteristics were shown in Table 1, and laboratory informations were shown in Table 2.
![]()
Figure 1. The pathology of the cervical lymph nodes. (A) (40×), Circumscribed sheets of histiocytes were accompanied by detrital necrosis, and coagulation necrosis can be seen locally. (B) (400×), Histiocytes stain positive with myeloperoxidase immunohistochemical stain. (C) (100×), in the xanthomatous phase of disease numerous foamy histiocytes were seen without prominent necrosis. (D) (100×), CD3 and CD5 immunohistochemistry of tissue cells in the diseased area were positive.
![]()
Table 1. Characteristics of KFD in six children.
![]()
Table 2. Laboratory results of KFD in six children.
4. Discussion
Since Kikuchi-Fujimoto disease was first discovered in Japan, more and more researchers have joined the research on this disease. Based on literature study, among adults, HNL is predominantly female, with a ratio of 4:1 [4]. However, studies on children find that the ratio of males is larger, with a ratio of 1.13:1, and the average age of children range from 11 to 13.2 years [3]. The average age in this study was similar with that reported in literatures but the subjects were all girls, which might be due to the lack of comprehensiveness of the data.
There are currently two most common viewpoints of its etiology: viral infection and autoimmunity. HNL clinical manifestations and antibiotics are similar to viral infections. Posterior cervical lymphadenopathy (mainly unilateral and V zone) and fever are the main clinical manifestations of KFD [5], and rare symptoms include weight loss, nausea, vomiting, rash, and upper respiratory symptoms [6] [7]. However, there was only one patient with viral infection in this study, and there was no research on the direct relationship between viral infections and KFD [8] [9]. In addition, there are reports that KFD is related to many autoimmune diseases, such as SLE, dry syndrome, Wegener granuloma, etc. [10] [11]. The researchers find that HNL patients are mainly concentrated in Asia, with certain genetic susceptibility. KFD enables T cells to induce immune responses to multiple antigens in gene susceptible individuals, and the study of KFD patients find that they often carry human white blood cells DPA1 and DPB1 of the antigens (HLA) II alleles [12].
For most children with cervical lymphadenopathy, ultrasound is the best diagnostic tool because it has no radiation and is non-invasive. When the affected lymph nodes are examined by ultrasound, hypoechoic foci are visible, and thick and irregular hyperechoic rings are visible on the outside [10]. However, ultrasonography is of limited value in the internal necrosis of lymph nodes, but CT scans can show extensive gross necrosis of diseased lymph nodes. The most common CT features of KFD in children are multiple, small, medium oval lymph nodes and round lymph node clusters related to internal necrosis [13]. 18F-FDG PET/CT may be useful in assessing KFD severity [14]. In terms of laboratory examination, children with KFD mostly showed decreased white blood cells and neutrophil counts. In addition, some children had abnormal liver enzymes and elevated ESR [3], which was consistent with the laboratory performance of children in this study. However, these manifestations are not specific.
As a self-limiting disease, most of KFD is currently diagnosed by histopathology and immunohistochemical examination of the affected lymph nodes. Involved lymph nodes are usually isolated, solid, mobile, painful but not purulent. Histologically, the lesions of the lymph nodes are mainly concentrated in the paracortical area, the structure of the lymph nodes is missing, the necrotic foci show a great deal of nuclear debris, and there are so-called crescent tissue cells. Among the tissue cells, small lymphocytes, activated T cells and plasma cells can be seen, and a large number of tissue cells accumulate at the edge of necrosis. The isolated apoptotic cells are scattered in large tissue cells, mixed with cell debris and nuclear dust. In addition, plasmacytoid dendritic cells (pDCs) and immunoblasts can also be seen, thromboangiitis are distributed around the necrosis. Among them, the obvious lack of neutrophils, eosinophils and plasma cells are characteristic lesions and have great diagnostic value. The tissue cells in KFD are positive for lysozyme, myeloperoxidase, CD68, CD163 and CD4. The lymphocytes in the lesion are mainly T cells, mainly CD8. Compared with CD4, there are very few CD20-positive B cells [2] [10] [15]. A large number of CD8-positive cytotoxic T cells in lymphoid follicles are related to FDC network changes. The rich and distorted FDC network structure spans all morphological patterns, which can be regarded as important supporting diagnostic evidence for KFD [16]. According to histological characteristics, the researchers find that KFD can be divided into three histological patterns: hyperplasia, necrosis and xanthoma [17].
Patients can fully recover on their own within a few weeks to several months, while cervical lymphadenitis can last for 6 months to 1 year. Approximately 3% - 4% of adults can relapse, but studies have found that children with KFD have a higher recurrence rate of 42.4% [18]. Symptomatic and supportive treatment is an effective means to relieve symptoms of persistent fever and pain, including glucocorticoids, intravenous immunoglobulin, or hydroxychloroquine. Studies have found that removing the affected lymph nodes is effective for treatment [3]. Most KFD patients quickly relieve their symptoms after taking glucocorticoids. A small number of patients with severe illness or poor response to glucocorticoids can receive intravenous immunoglobulin [19] [20]. Hydroxychloroquine has also been used in the treatment of KFD, which has a certain effect on some patients with refractory KFD, but there is no clear guidance on the dosage and course of treatment [11]. The current research shows that the prognosis of children is usually better than that of adults. Although most patients with KFD have a good prognosis, there are also a few that can develop into other diseases, such as autoimmune hepatitis, SLE, Sjogren’s syndrome, hemophagocytic syndrome, mixed connective tissue disease, etc. have been reported. Therefore, long-term follow-up is required [21]. In a few cases, children with KFD may have neurological complications, such as meningoencephalitis, cerebellar ataxia, and encephalitis with central nervous system disease [22]. For patients with nervous system involvement, it is necessary to control intracranial pressure and convulsions. The sample size of this study is small, and the reference to children’s HNL is limited, and the sample size needs to be expanded for further study.
5. Conclusion
As a rare disease, KFD has brought huge diagnostic challenges to clinicians. Due to the lack of specific clinical manifestations, laboratory examinations and imaging findings, most children will receive treatment for diseases such as anti-infection and anti-tuberculosis before diagnosis. What’s more, KFD is diagnosed by histopathology and immunohistochemical examination of the affected lymph nodes, and the removal of the affected lymph nodes has a therapeutic effect. Due to the self-limiting nature of the disease, most children have a good prognosis, but required long-term follow-up.
Data Declaration
The authors confirm that no prior presentation of the study data as an abstract or poster has taken place.