Neuroma: Difference between revisions

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:*T2: typically low signal but can sometimes be intermediate in signal
:*T2: typically low signal but can sometimes be intermediate in signal
:*T1 C+ (Gd): tends to show intense enhancement
:*T1 C+ (Gd): tends to show intense enhancement
=== Other Diagnostic Studies ===
*Neuroma  may also be diagnosed using [diagnostic study name].
*Findings on [diagnostic study name] include [finding 1], [finding 2], and [finding 3].


== Treatment ==
== Treatment ==

Revision as of 15:54, 21 April 2016

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List of terms related to Neuroma

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Maria Fernanda Villarreal, M.D. [2]

Synonyms and keywords: Traumatic neuroma; Morton neuroma; Joplin neuroma

Overview

Neuroma (Neuro- is from the Greek for nerve) is defined as a benign tumor of a nerve. However, neuroma commonly refers to any tumor of cells of the nervous system and forms a part of peripheral nerve sheath tumors.

Historical Perspective

  • Neuroma was first described by Thomas Morton in 1876

Classification

  • Neuroma may be classified according to histopathological features into 3 groups:
  • Morton neuroma
  • Symptomatic perineural fibrosis around a plantar digital nerve of the foot
  • Also known as Morton’s metatarsalgia
  • Traumatic neuroma
  • Arises from nerve injury (often as a result of surgery).
  • They occur at the end of injured nerve fibres as a form of uneffective, unregulated nerve regeneration
  • Subtype of traumatic neuroma, called "Joplin neuroma" (a compression traumatic neuroma)
  • Occurs most commonly near a scar
  • Often very painful
  • Neoplasic neuroma
  • Solid nodular mass
  • Usually, separate from nerve fibers

Pathophysiology

  • The pathogenesis of neuroma is characterised by neural degeneration with epineural and endoneural vascular hyalinization, and perineural fibrosis.
  • The pathogenesis of traumatic neuroma is characterised by a chronic reactive fibroinflammatory disorganised regeneration around a nerve after an injury (such as traction injury or chronic repetitive stress)
  • Morton neuroma is characterized by being located in the 3rd web-space, between 3rd and 4th metatarsal heads.
  • Another subtype of traumatic neuroma is terminal neuroma (also known as "stump neuroma") which can occur after transection of the nerve (e.g. limb amputation).
  • The are no genetic mutations associated with the development of neuroma.
  • On gross pathology, characteristic findings of neuroma, include:
  • Adherent fibrofatty tissue
  • Yellowish small mass
  • On microscopic histopathological analysis, characteristic findings of neuroma, include:
  • Extensive fibrosis around and within the nerve
  • Digital artery
  • Thrombosis
  • Arterial thickening

Causes

  • Common causes of neuroma, include:
  • Indirect nerve trauma
  • Traction injury
  • Chronic repetitive stress

Differentiating Neuroma from other Diseases

  • Neuroma must be differentiated from other diseases that cause forefoot pain, and numbness, such as:
  • Stress fracture (neck of the metatarsal)
  • Rheumatoid arthritis
  • Plexiform neurofibroma
  • Hammertoe

Epidemiology and Demographics

  • Neuroma is a uncommon disease.

Age

  • Neuroma is more commonly observed among patients aged between 15 to 50 years old.
  • Neuroma is more commonly observed among middle aged adults.

Gender

  • Females are more commonly affected with neuroma than males.
  • The female to male ratio is approximately 5:1.

Race

  • There is no racial predilection for neuroma.

Risk Factors

  • Common risk factors in the development of neuroma, include:

Natural History, Complications and Prognosis

  • The majority of patients with neuroma are symptomatic at the time of diagnosis.
  • Early clinical features include neuropathic pain, or local tenderness.
  • If left untreated, the majority of patients with neuroma may progress to develop walking difficulty, and limping.
  • The most important complication of neuroma is chronic neuropathic pain.
  • Prognosis is generally good, and the survival rate of patients with neuroma is 99%.

Diagnosis

Symptoms

  • Neuroma is usually asymptomatic.
  • Symptoms of neuroma may include the following:
  • Focal area of pain


Physical Examination

  • Patients with neuroma usually appear with antalgic posture.
  • Physical examination may be remarkable for:
  • Tenderness to palpation

Laboratory Findings

  • There are no specific laboratory findings associated with neuroma.


Imaging Findings

  • On ultrasound, neuroma is characterized by the following findings:
  • Round to ovoid
  • Well-defined, hypoechoic lesion
  • Located in the intermetatarsal space proximal to the metatarsal head
  • On MRI, characteristic findings of neuroma, include:
  • Dumbbell/ovoid-shaped lesion at a similar position to that described on ultrasound
  • T1: typically low-to-iso signal
  • T2: typically low signal but can sometimes be intermediate in signal
  • T1 C+ (Gd): tends to show intense enhancement

Treatment

Medical Therapy

  • Medical therapy for neuroma, include:
  • Ultrasound-guided interdigital injection of steroid and local anaesthetic.

Surgery

  • Surgery is the mainstay of therapy for neuroma .
  • Surgical excision is the treatment of choice for patients with neuroma with a relatively good success rate, around 80%.

Prevention

  • There are no primary preventive measures available for neuroma.
  • Secondary prevention measures, include: personal hygiene measures, such as wearing ergonomic shoes.

References