2014
DOI: 10.1016/j.jaad.2013.11.024
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Primary and secondary intralymphatic histiocytosis

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Cited by 32 publications
(50 citation statements)
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“…Clinically, intralymphatic histiocytosis presents with isolated asymmetrical plaques, macules or nodules. It has been included within the reactive angiomatoses and has recently divided into a primary and secondary forms, the latter associated with systemic diseases, notably rheumatoid arthritis (RA) . Other associated conditions include chronic inflammatory diseases, metal implantation, malignancy, especially breast cancer, and infection.…”
Section: Characteristics Of Patients With Intralymphatic Histiocytosismentioning
confidence: 99%
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“…Clinically, intralymphatic histiocytosis presents with isolated asymmetrical plaques, macules or nodules. It has been included within the reactive angiomatoses and has recently divided into a primary and secondary forms, the latter associated with systemic diseases, notably rheumatoid arthritis (RA) . Other associated conditions include chronic inflammatory diseases, metal implantation, malignancy, especially breast cancer, and infection.…”
Section: Characteristics Of Patients With Intralymphatic Histiocytosismentioning
confidence: 99%
“…Six reported patients (10.7%) had malignancies, 2 (3.6%) were associated with bacterial infection, tonsillitis and vulva necrosis and 11 (19.6%) were idiopathic. Other associated systemic conditions included Crohn disease, dermatomyositis and monoclonal gammopathy . Among malignancy associated intralymphatic histiocytosis, the most common observed tumor was breast cancer, with involvement presenting as erythematous patches developing on mastectomy scars .…”
Section: Characteristics Of Patients With Intralymphatic Histiocytosismentioning
confidence: 99%
See 1 more Smart Citation
“…The main differential diagnosis should be made with ILH and diffuse dermal angiomatosis of the breast, although intravascular (blood vessel) histiocytosis (IBH) is not intralymphatic, nor an angiomatosis. Nevertheless, it is remarkable that, in all cases, including the possible case reported previously in the literature, the breasts were involved, and in two cases they were the only location.…”
Section: Discussionmentioning
confidence: 99%
“…Intralymphatic lymphohistiocytic proliferations are relatively common, and different types have been described in recent years. In most cases the cause is intralymphatic histiocytosis (ILH), that may be either primary (idiopathic) or secondary to neoplastic diseases or inflammatory conditions, and is particularly frequent in relation to rheumatoid arthritis . In addition, different types of CD30 + lymphoproliferative disorders may also show lymphotrophism, including anaplastic large cell lymphomas, lymphomatoid papulosis and the incidental finding of benign clusters of T lymphoid blasts in the setting of inflammation .…”
Section: Introductionmentioning
confidence: 99%