Associated with EBV-associated B cell lymphoproliferative disorder, the
pathogenesis of which was suggested to be closely associated with immunosuppressive
treatment for progressive systemic sclerosisref.
Laboratory examinations :
distinguishing AILT from PTCLu can often be difficult; however, morphologic
features favoring AILT are prominent vascularization by arborizing venules,
expansion of CD21+ follicular dendritic cell networks, and the
recent identification of CD10 as phenotypic marker of the neoplastic T
cellsref.
An oligoclonal or monoclonal B-cell population due to the expansion of
B cells infected with EBV and secondary EBV+ B-cell lymphomas
has been described in some patients (Banks PM, Warnke RA. Mature T-cell
and NK-cell neoplasms. In: Jaffe ES, Harris NL, Stein H, Vardiman JW, eds.
World Health Organization Classification of Tumours: Pathology and Genetics
of Tumours of Hematopoetic and lymphoid Tissues. IARC Press: Lyon; 2001:189–230)
Prognosis : the outcome of AILT is poor, with
most series reporting a 5-year OS of approximately 30% and median survival
of 3 yearsref Therapy : anti-CD4
mAb
(HuMax-CD4 iv once weekly for 10 wkref)
angiocentric
immunoproliferative lesions (AIL): a multisystem disease with
adult onset, consisting of invasion and destruction of body structures
and tissue by atypical lymphocytoid and plasmacytoid cells resembling a
lymphoma; many affected patients develop frank lymphoma (mildly aggressive)
lethal
midline granuloma / polymorphic reticulosis : a progressive, localized,
destructive process occurring chiefly in males, predominantly involving
the nose, paranasal sinuses, and palate, with erosion through contiguous
structures such as the orbit and face and destruction of soft tissue, bone,
and cartilage, and associated with nonspecific acute and chronic inflammation
and necrosis with or without granuloma formation.
idiopathic midline granuloma : no neoplastic cells detected
lymphomatoid granulomatosis
: an immunoproliferative disorder that is angiogenic and characterized
by tissue infiltration and nodular granulomatous inflammation with atypical
lymphocytes and plasmacytoid cells; the organs involved are usually the
lungs, skin, central nervous system, or kidneys. Presenting symptoms include
cough, shortness of breath, and chest pain; extrapulmonary manifestations
are common, such as skin nodules => 50% develops malignant lymphoma
Aetiology : associated with HHV-4
/ EBV Laboratory examinations :