Differentials

Folic acid (vitamin B9) deficiency

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Generally does not present with neurological symptoms. Rare in the present era of folic acid fortification in the US.

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Serum folate levels are low.

Be aware that low serum folate can result in falsely low vitamin B12 levels.

Treat with folic acid and retest.

Myelodysplastic syndrome (MDS)

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Presents with macrocytic anaemia and is difficult to differentiate from vitamin B12 deficiency initially.

MDS is a group of disorders characterised by a clonal chromosomal abnormality, ineffective and dysplastic haematopoiesis resulting in ≥1 cytopenias, and a varying predilection to develop acute myeloid leukaemia.

These disorders can arise primarily without any precipitating event or may be related to previous treatment with either chemotherapy or radiation.

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FBC in MDS shows normochromic or macrocytic red cells; about 40% of patients have neutropenia, and >30% have thrombocytopenia. Morphological abnormalities include oval macrocytic red cells and granulocytes with the pseudo-Pelger-Huet anomaly (hypogranular and hypolobulated granulocytes).

Bone marrow histopathology in MDS demonstrates dysplasia in a proportion of undifferentiated myeloblasts.

Prussian blue iron staining of bone marrow aspirate can show ringed sideroblasts (abnormal erythroid precursor cells that have granules around the nucleus).

Alcoholic liver disease

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May present with macrocytic anaemia and nutritional deficiencies. History should reveal alcohol use.

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Elevated liver enzymes.

Liver biopsy histopathology shows fatty change, inflammation, and variable amounts of fibrosis leading to cirrhosis in severe, chronic alcoholic liver disease.

Hypothyroidism

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May present with macrocytic anaemia.

May show signs of muscle and joint pain, weakness in the extremities, and fatigue; delayed relaxation of deep tendon reflexes strongly suggests hypothyroidism.

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Elevated thyroid-stimulating hormone, decreased T3 and T4, and elevated creatine kinase.

Peripheral neuropathy

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Compression neuropathies, and neuropathies due to diabetes or thyroid disease, may be difficult to differentiate from neurological symptoms of vitamin B12 deficiency.

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Nerve conduction studies and electromyogram are helpful in confirming and characterising neuropathy; that is, demyelinating, axonal, polyneuropathy, mononeuropathy multiplex, radiculopathy, or plexopathy.

Treatment with vitamin B12 may improve symptoms, but neuropathy may be irreversible.

Diabetic neuropathy

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Paraesthesia is a common feature and may occur in the extremities as a result of neuropathy in those with prolonged undiagnosed diabetes. Other types of neuropathy may be present in diabetes, including autonomic neuropathy.

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Elevated fasting glucose or HbA1c.

Antiglutamic acid decarboxylase antibodies, islet cell antibodies, and insulin auto-antibodies are present in 85% of patients with type 1 diabetes at the time of diagnosis, but may disappear within a few years.

Drug-induced macrocytosis

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Macrocytosis due to certain medicines, including hydroxyurea, methotrexate, zidovudine, azathioprine, capecitabine, and cladribine.

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Usually a clinical diagnosis. Serum drug levels may confirm the association.

Dementia

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Characterised by cognitive (memory) changes, psychiatric symptoms, personality changes, problem behaviours, and changes in day-to-day functioning.

May be due to multiple different factors that are clinically indistinguishable from vitamin B12 deficiency.

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A mental state examination or neuropsychiatric testing should be conducted if the diagnosis is uncertain.

Vitamin B12 testing is normal.

Depression

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Characterised by persistent low mood causing varying levels of social, cognitive, occupational, and physical dysfunction.[78]

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Vitamin B12 testing is normal.

Pernicious anaemia (PA)

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Patients present with symptoms of anaemia and vitamin B12 deficiency. They may also have fever and complain of gastric pain or discomfort. Common features include tiredness, dyspnoea, paraesthesias, sore red tongue, diarrhoea, and mild jaundice.

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Once vitamin B12 deficiency is confirmed, testing for anti-intrinsic factor antibody (anti-IFAB) can determine whether PA is the cause. It is only 50% sensitive, but highly specific for PA.[2] Testing for anti-IFAB should be done before initiating vitamin B12 replacement therapy because high vitamin B12 levels may lead to false positive results.[70][71]

Antiparietal cell (APC) antibody can, in conjunction with other tests, help to determine whether PA is the cause. It is highly sensitive (85%), but has low specificity for PA. APC antibodies may be elevated in atrophic gastritis.[2]

Once a patient is given intrinsic factor, and vitamin B12 level is normal, gastrin levels will normalise.

Crohn's disease

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Crohn's disease can affect any part of the gastrointestinal tract, and symptoms may be extremely variable.

Increased risk for B12 deficiency occurs with ileectomy >20 cm.[47]

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The classic findings on histological examination include involvement of all layers of the bowel wall by granulomas, ulcerations, and acute and chronic inflammation.

Coeliac disease

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Patients present with unexplained gastrointestinal symptoms, chronic diarrhoea, unexplained iron-deficiency anaemia, vitamin D deficiency, or a skin rash consistent with dermatitis herpetiformis.

Other situations include failure to thrive, short stature, recurrent severe aphthous stomatitis, recurrent spontaneous abortion, and infertility.

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Immunoglobulin A antigliadin and anti-endomysial antibodies.

Small-bowel histology is the most specific and sensitive test, showing villous atrophy and mucosal inflammation with hyperplastic changes to crypts.

Iron-deficiency anaemia is the most common clinical presentation in adults.

Folate (and less commonly vitamin B12) deficiency may lead to macrocytic anaemia.

Peptic ulcer disease from Helicobacter pylori infection

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H pylori is a gram-negative, micro-aerophile bacterium that inhabits the stomach and duodenum. It causes a chronic low-level atrophic gastritis and is strongly linked to the development of duodenal and gastric ulcers and stomach cancer.

Over 80% of people infected with the bacterium are asymptomatic.

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The carbon urea breath test is positive.

The most reliable method for detecting H pylori infection is endoscopic biopsy. Histopathology shows gastric atrophy, inflammation, and bacterial organisms on special stains.

Chronic pancreatitis

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History of gallstone disease or alcohol misuse.

Characterised by recurrent or persistent abdominal pain and progressive injury to the pancreas and surrounding structures, resulting in scarring and loss of function.

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Ultrasound or CT imaging of the abdomen may reveal fibrosis and calcification of the pancreas.

Evaluation of pancreatic enzymes is the most sensitive and specific test for diagnosing mild-to-moderate pancreatic insufficiency or chronic pancreatitis, but it is available in only a few centres. Pancreatic juice is collected with a gastroduodenal tube during exogenous hormone stimulation with cholecystokinin and/or secretin.

Helps differentiate pancreatic from non-pancreatic types of malabsorption.

Small-intestinal bacterial overgrowth

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History may show conditions that alter intestinal anatomy, motility, and gastric acid secretion. These include use of proton-pump inhibitors and anatomical disturbances in the bowel, including fistulae, diverticula, and blind loops created after surgery.

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The definitive investigation requires culture of jejunal fluid that grows >10⁵ bacteria/mL.

Hydrogen breath testing may show malabsorption but is not very sensitive or specific for bacterial overgrowth.

A trial of treatment with antibiotics for 1 week may give the diagnosis.

Zollinger-Ellison syndrome

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A condition caused by a gastrin-secreting tumour that causes hypersecretion of gastric acid leading to ulcer disease. It most commonly presents with abdominal pain, diarrhoea, and gastro-oesophageal reflux. Less common presentations include weight loss, gastrointestinal bleeding, nausea, and vomiting.

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Elevated level of fasting serum gastrin in the absence of achlorhydria, and either a positive secretion test or histologically demonstrated neuroendocrine tumour.

Tropical sprue

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Believed to be initiated or sustained by an undefined infection.

Presents with symptoms and signs of malabsorption, stomach pain, diarrhoea, and bloating.

The relapse rate is substantial in treated patients who remain in, or return to, endemic areas in the tropics.

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Endoscopy and small bowel biopsy reveals progressive villus atrophy in the small intestine similar to coeliac disease.

Therapeutic trial with tetracyclines for 6 months normalises mucosal structure in the small intestine.

Fish tapeworm (Diphyllobothrium latum)

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Fish tapeworm is native to Scandinavia, western Russia, and the Baltic states. Now present in North America, especially the Pacific North-west.

Infection arises following eating raw fish or fish products.

Patients present with symptoms of malnutrition including anaemia.

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Fish tapeworm eggs appear in the faeces 5 to 6 weeks after infection, and faecal examination may confirm the diagnosis.

HIV infection

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Malnutrition is common in HIV disease, particularly in resource-poor areas. A cycle of opportunistic infection causing loss of weight and poor appetite, together with diarrhoea and malabsorption, contributes to malnutrition.

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Enzyme-linked immunosorbent assay (ELISA) testing should be ordered when HIV testing is indicated. False-negatives may occur during the window period immediately after infection and before antibodies to HIV have developed. A positive result should be confirmed with a Western blot or second ELISA. The window period can be reduced to 2-4 weeks by using fourth-generation tests that detect IgM and IgG antibodies to HIV and p24 antigen.[79] CDC: HIV - laboratory tests Opens in new window

Alpha-thalassaemia

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An inherited autosomal-recessive blood disease.

Vitamin B12 requirement is increased in alpha-thalassaemia; vitamin B12 deficiency may be the presenting feature. Patients present with anaemia, hepatosplenomegaly, leg ulcers, and bone pain. This disease is more common in Mediterranean countries, Asia, the Middle East, and South America.

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FBC and peripheral smear show microcytosis, erythrocytosis, hypochromia, and mild anaemia.

A diagnosis can be made by a combination of family studies and the ruling out of both iron-deficiency anaemia and beta-thalassaemia trait.

A definitive diagnosis can be made by DNA sequencing of the alpha-globin chain.

Multiple sclerosis

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Neurological manifestations of vitamin B12 deficiency can mimic clinical symptoms of multiple sclerosis. However, in almost all cases of multiple sclerosis there are also brain lesions.

Variable presentation: multiple episodes separated by space (i.e., neurological symptoms result from lesions in different central nervous system sites) and time. Symptoms include progressive limb weakness, gait difficulty, ataxia, loss of balance, and paroxysmal vertigo.

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Brain MRI typically shows areas of demyelination.

Cerebrospinal fluid (CSF) examination shows raised IgG and oligoclonal banding.

Syphilis (tabes dorsalis)

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History of syphilis infection or sexually transmitted infection.

Neurological symptoms of tabes dorsalis and sub-acute combined spinal degeneration may be similar.

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The Venereal Disease Research Laboratory (VDRL) reaction alone cannot always be depended on in differential diagnosis.

CSF examination is required to diagnose neurosyphilis.

CSF VDRL reactivity test is specific but not sensitive for neurosyphilis.

CSF fluorescent treponemal antibody absorption reactivity test is sensitive, but not specific for neurosyphilis.

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