Case Report Kikuchi's Lymphadenitis in Inguinal Lymph Nodes With

Case Report Kikuchi's Lymphadenitis in Inguinal Lymph Nodes With

Int J Clin Exp Med 2019;12(2):2025-2034 www.ijcem.com /ISSN:1940-5901/IJCEM0081108 Case Report Kikuchi’s lymphadenitis in inguinal lymph nodes with concurrent cutaneous squamous cell carcinoma Qionglan Tang1,2, Tingzhen Zhang1, Ping Liu8, Liping Ma3, Xiaoping Yuan4, Qiquan Wu8, Xinxin He1, Shaoyun Hao5, Shuling Zhou8, Weiqiang Liang6, Lie Dai7 1Department of Pathology, 2Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Departments of 3Hematology, 4Radiology, 5Ultrasound, 6Plastic Surgery, 7Rheumatology, Sun Yat- sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China; 8Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China Received June 10, 2018; Accepted November 12, 2018; Epub February 15, 2019; Published February 28, 2019 Abstract: The present study reports one case of combined Kikuchi’s lymphadenitis in inguinal lymph nodes and cutaneous squamous cell carcinoma (CSCC), along with a review of the literature. The patient was a 56-year-old man with a 3-year history of one gradually enlarging masses on the left lower leg. It developed from a brown plaque that had lasted for 10 years. Computed tomography (CT) revealed that an irregular mass infiltrated the surface of the left tibia. Ultrasound examinations showed the enlargement of many inguinal lymph nodes. Based on a radical resection of the leg mass and regional lymph node dissection, the diagnosis of Kikuchi’s lymphadenitis and primary CSCC without lymph node metastasis was made. Twenty-seven months after surgery, the patient remained in stable condition. The simultaneous occurrence of Kikuchi’s lymphadenitis with carcinoma is unusual and presents an interesting, challenging, and complex management dilemma. Keywords: Kikuchi’s lymphadenitis, carcinoma, coexistent disease Introduction mas (SCC) were collected from the Department of Pathology, Sun Yat-sen Memorial Hospital, Kikuchi’s lymphadenitis, also known as Kikuchi- Sun Yat-sen University, Guangzhou, China, be- Fujimoto lymphadenitis or histiocytic necrotiz- tween January 2012 and December 2017. All ing lymphadenitis, was first described in Japan cases were histologically and immunopheno- in 1972 [1, 2]. Its clinical and pathological fea- typically reviewed. Diagnosis was based on the tures of lymphadenopathy and necrotic lesions World Health Organization (WHO) classification are frequently misdiagnosed as other lymph of Pathology and Genetics of Skin Tumors node diseases, including primary and meta- (2006) [11], Tumors of Hematopoietic and Ly- static tumors. Previous studies have shown mphoid Tissues (2008) [12], and Hemato- that the simultaneous existence of Kikuchi’s pathology (2011) [13]. One case of Kikuchi’s lymphadenitis and carcinoma is extremely rare lymphadenitis and primary CSCC was identi- [3-10]. The current study presents one case of fied. Clinical and laboratory data of this patient combining Kikuchi’s lymphadenitis in inguinal were collected. Histological subtypes of Ki- lymph nodes and primary cutaneous squamous kuchi’s lymphadenitis and the histological cell carcinoma (CSCC), as well as a review of grade, tumor stage, and risk stratification of the literature. CSCC were evaluated [13-16]. Materials and methods Hematoxylin and eosin (HE) and immunohisto- chemical staining Patient selection Four micrometer-thick sections from formalin- Ninety-eight cases of Kikuchi’s lymphadenitis fixed paraffin-embedded blocks were cut for and 10,398 cases of squamous cell carcino- routine hematoxylin and eosin staining. The Kikuchi’s lymphadenitis with concurrent cutaneous squamous cell carcinoma EnVision method was used for immunohisto- clinical data. All experiments were repeated chemical staining (IHC) with diaminobenzidine three times. Differences were then discussed, (DAB) as a substrate. A broad panel of antibod- reaching a consensus. ies included: Leukocyte common antigen (LCA; RP2/18+RP2/22), Cluster of differentiation Review of the literature and statistical analysis (CD) 2 (AB75), CD3 (SP7), CD4 (SP35), CD5 (4C7), CD7 (272), CD8 (SP16), CD20 (L26), Articles from 1950 to 2018 containing the key- CD43 (DF-T1), CD56 (56C04), CD30 (Ber-H2), words “histiocytic necrotizing lymphadenitis” CD68 (KP1), CD123 (BR4MS), Anaplastic Ly- and “carcinoma” in PubMed, Scopus, Web of mphoma Kinase (ALK; 5A4), Granzyme B (GrB; Science, and GeenMedical databases were GZB01), T-cell intracytoplasmic antigen-1 (TIA- reviewed. All statistical analyses were per- 1; TIA-1), Cytokeratin (CK; MX005), CK5/6 formed using SPSS WIN program package 13.0 (D5/16B4), P63 (MX013), and Ki-67 nuclear (SPSS, Inc, Chicago, IL, USA). Survival times antigen (MIB-1). All antibodies were purchased were measured from primary diagnosis until from Beijing Zhongshan Biotechnology Co their censoring date. (Beijing; China). Slides were treated by pres- Ethical approval sure-cooking in a citric acid buffer (10 mM, Ph 6.0) for 3 minutes before staining for LCA, CD3, Each institution obtained approval to partici- CD4, CD5, CD7, CD8, CD20, CD43, CD56, pate in the study as required by the local Ethics CD68, ALK, GrB, TIA-1, CK, and P63 and in eth- Committee. Informed consent was obtained ylenediaminetetraacetic acid (EDTA; 1 mM, Ph from each patient and/or legal guardian. 9.0) for CD2, CD30, CD123, CK5/6, and Ki-67. Results In situ hybridization for EBV detection Clinical features of the patient In situ hybridization (ISH) was performed using a fluorescein isothiocyanate (FITC)-labeled co- A 56-year-old man was referred to Sun Yat-sen mmercial probe complementary to detect two Memorial Hospital, in January 2016, with a Epstein-Barr virus (EBV)-encoded small RNAs, 3-year history of one gradually enlarging mass- EBER-1 and EBER-2 (Y520001; Dako), follow- es with an ulceration on the lower left leg. It ed by a rabbit anti-FITC antibody conjugated developed from a brown plaque with occasion- with alkaline phosphatase (Dako) to combine al itching, no pain, and no purulence. It had with the probes. NBT/BCIP (nitroblue tetrazoli- lasted for 10 years. There was also an eight- um chloride/5-bromo-4-chloro-3-indolyl phos- year history of a brown plaque on the lower phate) was used as a substrate. Positivity could right leg, with occasional itching, no pain, and be observed in the nucleus as a blue-purple no purulence. One year ago, CSCC of the left signal. lower leg was first diagnosed by skin biopsy. However, the mass on the left lower leg seldom DNA extraction and polymerase chain reaction reduced in size after two cycles of paclitaxel DNA from paraffin-embedded tissue samples and cisplatin (TP) chemotherapy, 49 days of was extracted by phenol-chloroform proce- radiotherapy, and local Traditional Chinese dures. Polymerase chain reaction (PCR) was Medicine treatment for ten months. The patient performed using a multiplex PCR of European had suffered from hypertension and diabetes BIOMED 2 assays (Yuanqi Bio, Shanghai, China) for the past year. He had smoked cigarettes, 1 [17]. Primers for detecting clonally rearranged pack per day, and drank alcohol, about 0.5 kilo- immunoglobulin (Ig) were set in 8 multiplex PCR grams per day, for 30 years. He had no history tubes, including 5 Ig heavy locus (IGH; including of surgery, trauma, or ionizing radiation at the 3 variable joining domains and 2 diversity join- site of the lesion, no known family history of any ing domains), 2 Ig κ locus (IGK), and 1 Ig λ locus related diseases, no recurrent fever, no night (IGL). T-cell receptor (TCR) gene rearrangement sweats, and no weight loss in recent months. was performed using primers in 5 multiplex Upon physical examination, a black and brown, PCR tubes, including 3 TCRβ and 2 TCRγ. firm, unclear circumscribed, and ulcerated mass, measuring 10 cm×4 cm, was found on HE, IHC, EBV-ISH, and PCR detection was evalu- the left lower leg. A black and brown plaque, 10 ated by two independent observers blinded to cm×3 cm in size, without pain, itching, ulcers, 2026 Int J Clin Exp Med 2019;12(2):2025-2034 Kikuchi’s lymphadenitis with concurrent cutaneous squamous cell carcinoma Figure 1. Primary cutaneous squamous cell carcinoma of the left lower leg. A-D. CT scans. E. Gross cutaneous speci- men of left lower leg. F. Histopathology of squamous cell carcinoma (HE, Original magnification ×100). and bleeding, was found on the right lower leg. mm in depth, in the soft tissues. It infiltrated Multiple inguinal lymph nodes, without tender- the surface of the left tibia and was supplied ness or fixation, were palpable. His white blood with abundant blood by bifurcate vessels of the cell count was 7.43×109/L (normal value, 3.50- anterior and posterior tibial artery (Figure 9.50×109/L), red cell count was 3.13×1012/L 1A-D). Ultrasound examinations showed enlar- (normal value, 4.30-5.80×1012/L), Hemoglobin gement of many inguinal lymph nodes (Figure was 99 g/L (normal value, 130-175 g/L), plate- 2A), with no enlargement of the liver and let count was 390×109/L (normal value, 125- spleen. There were no abnormalities in the 350×109/L), and his monocyte proportion and lungs, according to chest radiography. count were 16.2% (normal value, normal 3.0- Pathological features of the patient 10%) and 1.2×109/L (normal value, 0.10- 9 0.60×10 /L), respectively. No abnormalities of Based on a radical resection of the leg mass the leukocytes, immunoglobulin G (IgE), IgG, and regional lymph node dissection, this case C3, C4, anti-dsDNA, anti-SSA, anti-SSB, anti- was diagnosed as Kikuchi’s lymphadenitis and neutrophil cytoplastic antibodies (ANCA), and primary CSCC. Regarding CSCC, there was a anti-nuclear antibodies (ANA) were detected. white or tan solid mass on the cut surface, C-reactive protein of 51.46 mg/L (normal value, measuring approximately 8.6 cm×4.8 cm×1.4 0.00-3.00 mg/L) was elevated and lactate cm in epidermis, which was exophytic growth dehydrogenase (LDH) levels were normal (163 with invasiveness, necrosis and ulcers, and U/L, normal 108-252 U/L).

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