Introduction
An elderly woman was seen for evaluation of a pruritic rash on her trunk and proximal
extremities. Clinically and histologically the lesions resembled mycosis fungoides
(MF). Two additional lesions on her back, with differing morphology, were proven to
be cutaneous B-cell lymphoma on pathology and gene rearrangement. Several case reports
have shown that MF is a risk factor for the development of a secondary B-cell lymphoma.
However, it is extremely rare for the two discordant lymphomas to present simultaneously
in the same patient.
Case report
An 81-year-old immunocompetent woman presented to the dermatology department on referral
from her primary care physician for treatment of a pruritic rash. The rash had been
present on her trunk for approximately 18 months, and to the knowledge of the patient,
the lesions all presented at the same time. She otherwise felt well with no complaints
of fevers, chills, night sweats, or weight loss. Upon examination, the patient was
found to have multiple pink, scaly patches and plaques clinically suggestive of MF
on the trunk and bilateral axillae (Fig 1) in addition to 2 erythematous, indurated
plaques on the mid back (Fig 2). There was no palpable lymphadenopathy or hepatosplenomegaly.
A biopsy of the plaque at the right portion of the upper chest, stained with hematoxylin-eosin,
found enlarged lymphocytes with hyperchromatic irregular nuclei. Epidermotropism and
focal Pautrier microabscesses were present. The papillary dermis was hyalinized. The
lymphocytes were highlighted on CD3 staining, and most cells expressed CD4 with little
CD8 expression. No significant CD20 staining was present. Periodic acidised CD4 staining
was negative for fungal organisms. The histologic findings were consistent with MF.
Biopsies of the right and left mid back found a dense, diffuse infiltrate of predominantly
lymphocytes with histiocytes and occasional plasma cells. The lymphocytes were not
significantly enlarged and had angulated to round nuclei and inconspicuous nucleoli.
CD20 and CD79a highlighted most of the lymphocytes and a smaller population of CD3+
lymphocytes was seen at the base of the lesion. Kappa and Lambda staining highlighted
plasma cells, but no significant clonal shift was identified. B- and T-cell gene rearrangement
was performed, and a B-cell (IgH) clone was identified. Additional immunostaining
was performed and the morphologic features, together with the immunophenotype (CD20+,
CD79a+, bcl6+, bcl2+partial, CD10−) and identification of a B-cell clone, was most
suggestive of a low-grade B-cell lymphoma (Fig 3, Fig 4). In situ hybridization stain
for Epstein Barr virus was also performed, and results were negative.
On referral to the oncology department, laboratory results showed a white blood cell
count of 6,760, hemoglobin of 12.5, platelet count of 127,000, and basophilia with
a basophil count of 3.8%. Sezary cell count showed 5% lymphocytes with features consistent
with Sezary cells. Computed tomography scan of the chest found a 3.3-cm enlarged node
in the preaortic space, small bilateral axillary adenopathy, and small bilateral pulmonary
nodules worrisome for metastatic disease. Bone marrow biopsy found increased numbers
of T cells both in small lymphoid aggregates and scattered diffusely through the marrow.
Flow cytometry found gating on 19% of cells, 87% CD3, 73% CD4/CD3, and 10% CD8/CD3.
Left axillary lymph node histology found small to medium lymphoid cells with some
nuclear irregularity and inconspicuous nucleoli. The cells showed lack of expression
of CD30 on immunohistochemical staining. Cytometry found an abundance of T lymphocytes,
of which most expressed CD4 and were negative for CD8. The cells also expressed CD2,
CD3, CD5, and CD7. The staging for her T-cell lymphoma was stage IVb.
The patient was initially treated with pazopanib and experienced no improvement after
2 months of 200-mg daily therapy. Cyclosporine and cyclophosphamide were also considered
as treatment options. Because of persistent and significant pruritus, the patient
was started on systemic psoralen and ultraviolet A therapy which provided symptomatic
improvement. Further systemic chemotherapy was offered and declined by the patient.
Discussion
Lymphomas coexisting in the same patient are classified by the Working Formulation
of non-Hodgkins lymphomas into three categories.
1
Discordant lymphomas are two histologically distinct lymphomas at two different anatomic
sites. Composite lymphomas have two types of lymphoma within the same anatomic lesion.
Lymphomas may also occur sequentially in which the second is known as secondary lymphoma.
Several cases in the literature report MF as a risk factor for secondary non-Hodgkins
lymphomas, and, rarely, Hodgkins lymphomas.2, 3, 4, 5, 6, 7, 8 Explanations have been
proposed for this association; the use of immunosuppressants in the treatment of the
primary lesion, a genetic predisposition to malignancy, and the monoclonal proliferation
of T cells in MF modulating the B-cell system, have all been implicated in causing
secondary malignancies.
9
The Epstein-Barr virus has also been implicated in driving a B-cell lymphoproliferative
process in patients with MF; the Epstein Barr virus studies in our patient were negative.
10
Although it is a well known, yet rare, occurrence for MF to present with a secondary
B-cell malignancy, it is exceedingly rare to find the two presenting simultaneously.
Our patient presented with discordant cutaneous lymphomas in two anatomically distinct
locations occurring roughly within the same timeframe. There are no documented cases
of simultaneous presentation of discordant cutaneous lymphomas, to our knowledge,
as most occur as a secondary lymphoma.
Our case further supports the need to perform multiple biopsies when patients present
with morphologically different cutaneous findings.