Kimura’s disease (KD), mostly seen in young Asian boys, typically manifests with subcutaneous lesions and cervical lymphadenopathy. It has a good prognosis and has no risk of malignancy. Inguinal lymphadenopathy is rarely reported as a presenting feature of KD. Here we report such a case of KD in an 11-year old girl. The diagnosis of KD was confirmed in this case by characteristic histopathological findings of the excised lymph node.
KimmHTSzetoC. Eosinophilic hyperplastic lymphogranuloma, comparison with Mikulicz’s disease. Proc Chin Med Soc1937; 1: 329–329.
4.
JaniACoulsonM. Kimura’s disease: A typical case of a rare disorder. West J Med1997; 166: 142–144.
5.
ViswanathaB. Kimura’s disease in children: a 9 years prospective study. Int J Pediatr Otorhinolaryngol2007; 71: 1521–1525.
6.
ChenHThompsonLDAguileraNSAbbondanzoSL. Kimura disease: a clinicopathologic study of 21 cases. Am J Surg Pathol2004; 28: 505–513.
7.
Hsu SN, Chang CF, Su TF, Hsu YC, Chen YA and Chen HC. Kimura’s disease associated necrotizing eosinophilic vasculitis presenting with recurrent peripheral arterialocclusive disease: a case report and review of the literature. J Thromb Thrombolysis 2014 Jul 9. [Epub ahead of print].
ChowLTYuenRWTsuiWMaTKChowWBChanSK. Cytological features of Kimura’s disease in fine needle aspirates: A study of eight cases. Am J Clin Pathol1994; 102: 316–321.
Vaughan HudsonBLinchDCMacintyreEABennettMHMacLennanKAVaughan HudsonG. Selective peripheral blood eosinophilia associated with survival advantage in Hodgkin’s disease (BNLI Report No 31). British National Lymphoma Investigation. J Clin Pathol1987; 40: 247–250.
12.
KungITGibsonJBBannatynePM. Kimura’s disease: a clinico-pathological study of 21 cases and its distinction from angiolymphoid hyperplasia with eosinophilia. Pathology1984; 16: 39–44.
13.
IannuzziMCRybickiBATeirsteinAS. Sarcoidosis. N Engl J Med2007; 357: 2153–2165.