2001
DOI: 10.1046/j.1468-3083.2001.00310.x
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Histiocytic necrotizing lymphadenitis preceding systemic lupus erythematosus

Abstract: Necrotizing histiocytic lymphadenopathy (NHL) is a rarely observed clinical entity that is occasionally associated with systemic lupus erythematosus (SLE). The histological features of the condition have been considered to be indistinguishable from those of lymphadenitis in subjects with SLE, and the clinical symptoms of the two disorders share common features. This report presents the case history of a subject who developed SLE with central nervous system involvement 3 years following onset of Kikuchi's disea… Show more

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Cited by 13 publications
(4 citation statements)
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“…13,14 Some patients who had recurrent HNL did not show any skin lesions when they were first diagnosed with HNL. 15,16 However, when these patients were diagnosed with SLE, diverse skin lesions developed during the second episode of HNL, coexisting with SLE. These patients are similar to the presented case 9.…”
Section: Discussionmentioning
confidence: 99%
“…13,14 Some patients who had recurrent HNL did not show any skin lesions when they were first diagnosed with HNL. 15,16 However, when these patients were diagnosed with SLE, diverse skin lesions developed during the second episode of HNL, coexisting with SLE. These patients are similar to the presented case 9.…”
Section: Discussionmentioning
confidence: 99%
“…In reporting a new case of nodal and cutaneous KD, we reviewed the literature in order to seek reliable criteria for its differential diagnosis. To the best of our knowledge, 27 cases of nodal and cutaneous KD have been reported, including ours, and 28 of KD associated with LE (in 13 the diagnosis of KD preceded LE; in nine HNL followed it, and in six the diseases were concomitant) 1–15 . Our patient, an 18‐year‐old Nigerian woman with a history of multiple self‐limiting febrile episodes and idiopathic skin eruptions over the last 8 years, presented with a 2‐week history of fever, cervical and axillary lymphadenopathy, anaemia, leukopenia, and high erythrocyte sedimentation rate.…”
mentioning
confidence: 77%
“…HNL may occur in patients with preexisting SLE, 28 may coexist with SLE, [29][30][31][32] or may evolve into SLE. [33][34][35][36][37][38] Patients with self-limiting HNL, also known as KD, can have a presentation with fever, skin lesions and subacute lymphadenopathy, mimicking SLE clinically and histologically. Whereas KD is mainly limited to lymph nodes, LErelated HNL is more frequently accompanied by cutaneous lesions.…”
Section: Discussionmentioning
confidence: 99%