By Disease Name > Pseudolymphoma

Pseudolymphoma

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B-cell pseudolymphoma regarded as a distinct clinical entity

(idiopathic) lymphocytoma cutis
borrelial lymphocytoma cutis

 

T-cell pseudolymphoma a heterogeneous group of diseases rather than a diagnosis sui generis;

drug
arthropod
actinic reticuloid
+/- Jessners
+/- LyP (= “a T-cell infiltrate of unpredictable behavior”)

 

 

hmtoggle_plus1HISTOLOGY:

B-cell  = nodular

 

T-cell  = two patterns

band-like (major pattern) AKA  MF-like

type B LyP
actinic reticuloid
lymphomatoid drug eruptions (most)

nodular (minor pattern)

type A LyP
persistent bite reaction (most)

 

mnemonic:

A,A is nodular   (type A LyP and arthropod bite)
B,C and D are band-like (type B LyP, CAD, drug)

 

hmtoggle_plus1IMMUNOHISTOCHEMISTRY:

Cutaneous T-cell Pseudolymphoma:

as in most cases of CTCL, the lymphocytes in CTPL are CD4+
exception = actinic reticuloid (CD8+)
loss of pan-T-cell markers (CD2, CD3, CD5) described in CTCL, has not been reported in CTPL
loss of CD7, common in CTCL, is rare in CTPL

 

Cutaneous B-cell Pseudolymphoma:

λ and κ light chains
polyclonal in CBPL
one predominates (>10:1 or <0.5:1) in CBCL

 

monoclonal antibodies to bcl-2 protein and MT2 are useful markers in distinguishing primary cutaneous follicular lymphomas from CBPL with germinal centers:

 

bcl-2 protein:

a proto-oncogene; blocks apoptosis
rarely seen in pseudolymphoma with germinal centers

 

MT2-CD45RA:

= an IgG antibody that reacts with antigens on both T and B lymphocytes of the mantle and marginal zone
expression is exclusively restricted to follicular lymphomas (i.e. specific)
low sensitivity ( 20%) therefore negative results do not exclude a malignant process