Differentials

Mantle cell lymphoma

SIGNS / SYMPTOMS
INVESTIGATIONS
SIGNS / SYMPTOMS

Clinically indistinguishable.

INVESTIGATIONS

Biopsy specimen shows absence of transformed blasts; immunohistochemistry shows CD5, IgD, and cyclin D1 positivity; cytogenetic testing shows t(11;14).[23][32]

Chronic lymphocytic leukaemia/small lymphocytic lymphoma

SIGNS / SYMPTOMS
INVESTIGATIONS
SIGNS / SYMPTOMS

Typical clinical features include painless lymphadenopathy, with or without B symptoms. Gastrointestinal disease is uncommon.

INVESTIGATIONS

Immunohistochemistry shows CD5, LEF1, and CD23 positivity; cytogenetic testing often shows del(13q) or trisomy 12; bone marrow biopsy usually shows bone marrow involvement.[23]

Follicular lymphoma

SIGNS / SYMPTOMS
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SIGNS / SYMPTOMS

Almost always presents with nodal disease. Extranodal disease is uncommon.

Most patients have widespread disease at presentation, enlarged lymph nodes (typically Waldeyer's ring and cervical lymph nodes), and splenomegaly.[23] Occasionally can present with palpable masses in the abdomen and abdominal pain or GI bleeding.

INVESTIGATIONS

Immunohistochemistry shows CD10 and BCL6 positivity in tumour cells within and between follicles; bone marrow biopsy usually demonstrates bone marrow involvement.[23]

Diffuse large B-cell lymphoma

SIGNS / SYMPTOMS
INVESTIGATIONS
SIGNS / SYMPTOMS

Symptoms are aggressive, with abdominal pain, vomiting, and haematemesis occurring more commonly than with gastric MALT lymphoma.

INVESTIGATIONS

Biopsy shows medium- to large-sized tumour cells; proliferative index (e.g., Ki-67) is high.

Peptic ulcer disease

SIGNS / SYMPTOMS
INVESTIGATIONS
SIGNS / SYMPTOMS

Clinically indistinguishable from gastric MALT lymphoma.

INVESTIGATIONS

Molecular testing for immunoglobulin gene rearrangement may help distinguish malignant (clonal) lymphoma from benign (polyclonal) conditions (e.g., hyperplasia, chronic inflammation). In some cases monoclonality can be demonstrated in uncomplicated chronic gastritis, and this may precede the emergence of gastric MALT lymphoma.[39][40] 

Chromosomal translocations and histopathological examination of the stomach can differentiate MALT lymphoma from peptic ulcer disease.

Hashimoto's thyroiditis

SIGNS / SYMPTOMS
INVESTIGATIONS
SIGNS / SYMPTOMS

Causes hypothyroidism that is usually insidious in onset, with signs and symptoms slowly progressing over months to years.

Some of the common symptoms of hypothyroidism include cold intolerance, voice hoarsenesss, painless goiter, pressure symptoms in the neck from thyroid enlargement, slowed movement and loss of energy, menstrual irregularities (typically menorrhagia, infertility, and loss of libido), depression, dementia, and other psychiatric disturbances, as well as memory loss.

INVESTIGATIONS

Elevated TSH with low free T4 levels; antithyroid peroxidase (anti-TPO) and antithyroglobulin (anti-Tg) antibodies are positive in the majority of cases.

Lymphoepithelial sialadenitis

SIGNS / SYMPTOMS
INVESTIGATIONS
SIGNS / SYMPTOMS

Clinically indistinguishable from salivary/parotid gland MALT lymphoma.

INVESTIGATIONS

Biopsy of the salivary glands shows a spectrum of histopathological features including: 1) fully benign lymphoid infiltrate, with or without an associated lymphoid follicular structure, without immunoglobulin (Ig) light chain restriction in B cells, and without any features of aggressive behaviour; 2) lymphoproliferative lesions, with or without areas of Ig light chain restriction in B-cells, with the usual presence of centrocyte-like cells. A more or less pronounced lymphoepithelial aggressiveness may be present without definite evidence of malignancy.

B-cell clones are detected in over 50% of cases by molecular genetic methods but this does not correlate with morphological or clinical evidence of overt lymphoma.

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