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Feline extramedullary
plasmacytoma (EMP)
©M.
Majzoub, W. Breuer, S. J. Platz, R. P.
Linke, W. Linke and W. Hermanns.
Histopathologic and Immunophenotypic Characterization of Extramedullary
Plasmacytomas in Nine Cats. Vet Pathol
40:249-253 (2003). http://www.vetpathology.org/cgi/content/full/40/3/249
Plasmacytomas are neoplasms consisting mainly of
plasma cells at varying stages of differentiation.11 The
solitary myeloma and multiple myeloma are additional types of
plasma-cell–derived tumour. The latter are primarily located in the
bone marrow. Extramedullary plasmacytomas (EMPs) are characterized by
their extraskeletal location.8,29
As defined by the World Health Organization, EMPs consist of atypical
neoplastic plasma cells with monoclonal expression of immunoglobulin
(Ig) light chains or heavy chains.15 They differ from other
non-Hodgkin lymphomas by their predominantly post-mitotic and
terminally differentiated plasma cells. The main cellular function,
production and secretion of Igs, is largely unaffected.22
Whereas the EMP is a frequent neoplasm in dogs,4,13,16,23,25–27 it is
a sporadic tumour in man.3,7,29,30
Judging from the existing case reports involving only one or two
animals, the incidence of EMP in cats seems to be low. Feline EMPs
have been described as occurring in the skin,4,5,13,19
gastrointestinal tract,24,31
retroperitoneal space,14
upper lip, gingiva,9
and orbita.28
Affected cats were generally more than 10 years old; the average
age of the animals was 10.6 years.13,19
A male predisposition could be clearly concluded from the literature
(male to female ratio was 2:1). The European Short-Haired cat was the
most commonly affected. One case each was reported in the Abyssinian,28
the Long-Haired, the Persian,9
and the Burmese13
breeds. Tumour-associated monoclonal gammopathy was reported in three
cases.5,14,28
The literature is uniform in describing the
morphology as a monomorphic population of plasma cells with isolated
bi- or multinucleated giant cells.4,28,31
In several cases, immunohistochemistry revealed monoclonal expression
of λ-Ig light chains,4,6,9,19
whereas λ-Ig light-chain expression was found in only one case.9
Ig heavy chains of the immunoglobulin G (IgG)9
and immunoglobulin (IgA)31
types also have been confirmed in the tumour cells. Amyloid deposits
in feline EMPs were demonstrated by several authors,4,5,13,14,19,24
although the amyloid was identified as AL λ-amyloid in only three
cats.19,24
To exclude a multiple myeloma, some authors examined the bone marrow
for tumour cell infiltrates in the cats.5,10,14,31
In humans, the extramedullary plasmacytoma is
uncommon and accounts for less than 5% of all plasmacellular
neoplasia.7,29,30 Although EMPs are commonly found in
dogs, mostly in the form of skin and mucosal neoplasms,20
they seem to be rare in cats. The latter conclusion can be drawn both
from the fact that so far only single-case reports exist in the
literature and from the incidence of cutaneous EMPs, as estimated
from the number of biopsies submitted to this department for
histologic examination. The incidence of EMPs in other parts of the
body besides the skin remains unknown, although, according to other
authors, it can be assumed to be low.4,5,13 From our own
series, it also can be confirmed that EMPs in cats are mainly
cutaneous neoplasms, as observed previously.4,5,9,13 The
occurrence of EMPs in other organs, e.g., digestive tract 24,31
and liver,10 is rare. With an average age of 8.2 years,
the EMP occurs predominantly in older cats. This, as well as the
preference for the male sex, agrees with the result in the
literature.4,5,13
As in dogs, a typing of EMPs based on morphologic
criteria also is possible in cats. With the exception of the hyaline
type described in dogs, the same types of EMP found in dogs were
found in cats. The absent hyaline type might be found in cats,
if a larger number of tumours could be examined. Because of the small
number of cases and a lack of follow-up studies, no claim can be made
currently concerning the diagnostic significance of the typing of
feline EMPs.
Immunohistochemistry of the feline EMPs mainly
revealed λ light-chain expression. This is very similar to the
physiologic distribution of light chains in normal feline plasma
cells with primary expression of the λ light chain.1
Monoclonal λ light-chain expression was reported in only one case.9
With respect to the immunohistochemical results in our series, the
possibility that the tumour plasma cells could express Ig heavy
chains not detectable with the routinely used antibodies cannot be
excluded. According to the literature, amyloid is more frequently
found in feline EMPs than in canine EMPs. Six out of 12 published
cases of EMPs in cats report on amyloid deposits.4,5,14,19,24,28
In the present study, three of the nine EMPs contained amyloid,
identified as AL λ-amyloid. This is consistent with the result of the
only study published to date of an immunohistochemically investigated
feline EMP.24
As reported by other authors,5,10,14
immunohistochemical examination for FeLV-antigen (p27 protein) was
negative for all tumours. Communication of the above results may
contribute to the already existing knowledge regarding extramedullary
plasmacytomas in cats.
 |
Fig. 1.
Skin, paraffin section; European Short-Haired cat, 7-year-old spayed
female. Feline extramedullary plasmacytoma (EMP, asynchronous type of
tumour cells) with basophilic cytoplasm, a clear perinuclear halo, and a
blastic nucleus with a central nucleolus. Giemsa. Bar = 20 µm.
Fig. 2. Immunohistochemical demonstration of Ig-light-chains in the
cytoplasm of tumour cells. Same cat as in Fig. 1. Bar = 20 µm.
Fig. 3. Feline EMP with homogenous eosinophilic amyloid deposits.
HE. Bar = 50 µm.
Fig. 5. Skin; European Short-Haired cat, 13-year-old castrated
male. Congo red–staining of EMP, mature type of tumour cells. Bars = 20
µm.
Fig. 6. All Congo-red positive areas within the tumour are
identified as amyloid by green-birefringence in polarized light. Same cat
as in Fig. 5. Bars = 20 µm.
Fig. 7. Immunohistochemical identification of AL amyloid with the
anti-AL-λ antibody ULI. Same cat as in Fig. 1. Bar = 20 µm. |
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