Burning feet in polycythemia vera – peripheral sensorimotor axonal neuropathy with erythromelalgia

Abstract

Polycythemia vera is a rare myeloproliferative disease. Cutaneous symptoms are uncommon. We report about a 72-year-old female patient with JAK2^V617F-positive polycythemia who developed peripheral sensorimotor axonal neuropathy and erythromelalgia. Possible causes and treatment are discussed.

Introduction

Polycythemia vera (PV) is a hematologic disease that is characterized by accumulation of phenotypically normal red blood cells, white blood cells, and platelets. The disease is diagnosed by a combined approach of laboratory investigations, bone marrow histology, and detection of characteristic mutations.^1,2 A mutation of the JAK2 gene is found in 98% of PV patients and clearly distinguishes PV from secondary polycythemia.² The typical JAK2^V617F mutation induces a loss of inhibitory activity of the JH2 pseudokinase part on the JH1 of Janus kinase 2 (JAK2). This results in enhanced activity of JH1 kinase activity of JAK2. Mutated hematopoietic stem cells thereby become hypersensitive to their appropriate hematopoietic growth factors, resulting in myeloproliferation.²

PV is a rare disease. The annual incidence has been calculated to be from 0.01 to 2.61.³

Classical maintenance treatment consists of hydroxyurea and phlebotomy.^4,5 More recently, Janus kinase inhibitors have become available, with promising results in clinical trials.⁶ Antithrombotic drugs are used to decrease the risk of thromboembolic events.⁵ Cutaneous manifestations are uncommon in PV. We report a case of peripheral sensorimotor axonal neuropathy combined by erythromelalgia.

Case report

A 72-year-old woman presented with a history of burning feet that started about one year earlier. On examination there was a livid red discoloration on the soles of the feet (Figure 1). Her medical history was remarkable for a diagnosis of PV in April 2011. The diagnosis was based on elevated hemoglobin, hematocrit, and red cell mass. JAK2^V61F and PRV1 (polycythemia vera rubra-1) mutations were detected cytogenetically, excluding secondary erythrocytosis.

Figure 1.

Palmar erythema with slight edema. Toes are involved as well.

Routine laboratory investigation demonstrated normal blood glucose, transaminases, creatinine, thyroid hormones, and folate. Elevated were hematocrit (53%), leukocyte (11.4 Gpt/L), thrombocytes (410 Tpt/L), and serum vitamin B12 (920 pg/mL) levels. Paraproteinemia was excluded by electrophoresis. Vibratory testing with a tuning fork at 128 Hz was slightly decreased symmetrically on the distal part of the legs in a stocking-like pattern. Pinprick and proprioception were also decreased distally. The Achilles tendon reflex was absent. Dorsiflexion of the feet was weak, but patellar reflexes were present. Muscle hypotrophy was not obvious.

Previous treatment had consisted of antithrombotic drugs, acetylsalicylic acid and angrelide, and the cytoreductive compound hydroxycarbamide. Due to noncompliance, all medical treatments had to be stopped shortly after initiation. Thereafter, she received regular phlebectomy only. We suspected a diagnosis of erythromelalgia in combination with peripheral sensorimotor axonal neuropathy of the legs. The patient was referred for further diagnostics to the neurologist (Table 1).

Table 1.

Electrophysiological findings

	Left	Right
Motor amplitude ≥5 mV	3.5	3.7
Distal motor latency ≤5 msec	5.65	5.43
Distal sensory latency ≤2.5 msec	3.01	3.18
Peroneal nerve velocity (m/sec)	42.1	41.3
Peroneal neural amplitude (mV)	4.3	4.2
Sural nerve velocity (m/sec)	44.1	43.4
Sural neuronal amplitude (mV)	7.2	7.0

Discussion

PV is a hematological disorder. Pruritus is the most frequent cutaneous symptom, with a negative impact on quality of life. A recent study in more than 400 PV patients reported aquagenic pruritus in 68.3% of patients. PV-associated pruritus does not respond to antihistamines, but can be treated with aspirin and paroxetine.⁷ Other cutaneous symptoms such as leg ulcers, livedo racemosa, and erythromelalgia are rare, and only case reports and case series have been published.^8–10

Erythromelalgia can be divided into a primary and secondary subtype. In the present case, we refer to secondary erythromelalgia. Clinically, erythromelalgia is characterized by a triad of erythema, increased local temperature, and burning pain. Histologically, erythromelalgia demonstrates capillary proliferation, endothelial swelling, perivascular edema, and sparse lymphocytic infiltrates.¹⁰ Redness and burning pain were present in our patient but elevated temperature was missing. Symptoms were unresponsive to aspirin but the patient was also noncompliant.

Our patient had additional signs of chronic symmetrical peripheral neuropathy with motor and sensory symptoms. We discussed the possibility of drug-induced peripheral neuropathy. Hydroxyurea-induced erythromelalgia is a very rare event.¹¹ Hydroxycarbamide has been reported to cause peripheral neuropathy when it is combined with didanoside and stavudine (as in human immunodeficiency virus). The effect is dose-dependent. Such combined medication was never given to the patient.

Hydroxycarbamide 600 mg/day has been considered safe.¹² The patient had taken hydroxycarbamide for no longer than 8 weeks, which makes this a rather unlikely cause. Acetylsalicyclic acid and angrelide are not known to cause neuropathy.

Therefore, we considered symmetrical peripheral sensorimotor axonal neuropathy as the underlying cause. Diagnosis of peripheral neuropathy in general follows a stepwise algorithm. In patients with signs and symptoms of chronic polyneuropathy and a typical clinical phenotype in association with a known cause of peripheral neuropathy, like diabetes or alcoholism, additional blood tests and electrophysiological studies are not informative. If there is no known cause, ancillary studies should initially aim at the identification of diabetes, alcohol misuse, or renal failure, all of which were negative in our patient. In the remaining patients, electrophysiological studies are recommended (Table 1).¹³

PV-associated neuropathy has been classified in group five of the peripheral neuropathies in the 1993 Amsterdam guideline.¹³ PV can cause neurological symptoms such as headaches, dizziness, and fatigue. None of these were present in our patient. On the other hand, PV is rarely associated with peripheral sensorimotor axonal neuropathy. The underlying mechanism is hypoxia due to blood hyperviscosity and abnormal platelet aggregation. Timely recognition of this symptom and more frequent phlebotomy may prevent severe damage.¹⁴ On the other hand, no relationship between severity of peripheral axonal neuropathy and duration of PV disease was found.¹⁴ Unfortunately, sensorimotor axonal neuropathy is irreversible.^14–16