Neurofibroma medical therapy: Difference between revisions

Jump to navigation Jump to search
No edit summary
Line 18: Line 18:


Removal of plexiform neurofibromas is difficult because they can be large and cross tissue boundaries.  However, besides pain, plexiform neurofibromas are sometimes removed due to the possibility of [[malignant transformation]].
Removal of plexiform neurofibromas is difficult because they can be large and cross tissue boundaries.  However, besides pain, plexiform neurofibromas are sometimes removed due to the possibility of [[malignant transformation]].
The following examples show that plexiform neurofibromas can form anywhere and can make surgical resection difficult:
* A large plexiform neurofibroma in the leg of a 6-year-old male. The authors state: “Our case was operated, as both the cutaneous and deep branches of the peroneal nerve were involved causing pain and numbness in the leg, and because there was a possibility for malignant transformation, as growth in the mass was realized by the family members of the patient.” In [[Wiktionary:in layman's terms|layman’s terms]], they decided to remove the neurofibroma because it was causing the boy pain and numbness in his leg, and because there was a possibility that it was undergoing a malignant transformation as his family noticed an increase in the tumor's size. The authors also note, “However, complete resection is quite difficult due to invasion of the tumor into the surrounding soft tissues.” <ref name=" pmid17377797">{{cite journal |author=Cebesoy O, Tutar E, Isik M, Arpacioglu O. |title=A case of isolated giant plexiform neurofibroma involving all branches of the common peroneal nerve |journal=Archives of Orthopaedic and Trauma Surgery |volume=127 |issue=8 |pages=709–12 |year=2007 |pmid=17377797|doi=10.1007/s00402-007-0303-1}}</ref>
* A neurofibroma on the [[left ventricle]]. The neurofibroma was removed and the patient’s [[mitral valve]] had to be replaced.<ref>{{cite journal  |vauthors=Iino K, Matsumoto Y, Endo M, etal |title=Surgical treatment of a left ventricular neurofibroma |journal=Journal of Cardiac Surgery |volume=21 |issue=3 |pages=278–80 |year=2006 |pmid=16684061 |doi=10.1111/j.1540-8191.2005.00135.x}}</ref>
* A 14-year-old girl with NF1 was diagnosed with a neurofibroma involving her bladder, a rare location.<ref name=" pmid18458838">{{cite journal |author=Meesa IR, Junewick JJ |title=Pelvic plexiform neurofibroma involving the urinary bladder |journal=Pediatric Radiology |volume=38 |issue=8 |pages=916 |date=August 2008  |pmid=18458838 |doi=10.1007/s00247-008-0865-2}}</ref>


====Radiation====
====Radiation====

Revision as of 18:48, 16 November 2015

Neurofibroma Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Neurofibroma from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

Diagnostic Study of Choice

Staging

History and Symptoms

Physical Examination

Laboratory Findings

X Ray

CT

MRI

Ultrasound

Other Imaging Findings

Other Diagnostic Studies

Treatment

Medical Therapy

Surgery

Primary Prevention

Secondary Prevention

Cost-Effectiveness of Therapy

Future or Investigational Therapies

Case Studies

Case #1

Neurofibroma medical therapy On the Web

Most recent articles

Most cited articles

Review articles

CME Programs

Powerpoint slides

Images

American Roentgen Ray Society Images of Neurofibroma medical therapy

All Images
X-rays
Echo & Ultrasound
CT Images
MRI

Ongoing Trials at Clinical Trials.gov

US National Guidelines Clearinghouse

NICE Guidance

FDA on Neurofibroma medical therapy

CDC on Neurofibroma medical therapy

Neurofibroma medical therapy in the news

Blogs on Neurofibroma medical therapy

Directions to Hospitals Treating Neurofibroma

Risk calculators and risk factors for Neurofibroma medical therapy

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Shanshan Cen, M.D. [2]

Overview

Treatment

Dermal neurofibroma

Dermal neurofibromas are not usually surgically removed unless they are painful or disfiguring, because there are generally so many of them and they are not dangerous.

CO2 lasers have been used to remove dermal neurofibromas. In a paper titled Hypertrophic Scars After Therapy with CO2 Laser for Treatment of Multiple Cutaneous Neurofibromas Ostertag et al. said this about treatment by laser: “The cosmetic disfigurement is the most important issue in the decision to treat cutaneous symptoms of neurofibromatosis. Treating patients with extensive neurofibromas with [a] CO2 laser is still the best choice. However, it is strongly advised that a test treatment be performed to judge the effectiveness of the procedure and whether the developed scar is an acceptable trade-off.” [1]

Plexiform neurofibroma

Surgery

As of 2002, the primary treatment option for plexiform neurofibroma was surgery.[2]

Removal of plexiform neurofibromas is difficult because they can be large and cross tissue boundaries. However, besides pain, plexiform neurofibromas are sometimes removed due to the possibility of malignant transformation.

Radiation

Once a plexiform neurofibroma has undergone malignant transformation, radiation and chemotherapy can be used as treatment. However, radiation is generally not used as a treatment for plexiform neurofibromas because of concerns that this could actually promote malignant transformation. There has even been a documented case of a Schwannoma being induced from a neurofibroma due to radiation therapy.[3]

Medications

ACE inhibitors have been proposed as a novel treatment of neurofibromas. ACE inhibitors are currently used to treat hypertension and congestive heart failure, to avert remodeling and reinfarction after myocardial infarction, and to ameliorate diabetic nephropathy and other renal diseases. ACE inhibitors work by indirectly down regulating TGF-beta, which is a growth factor that has been shown to influence the development of tumors.[4]


References

  1. Ostertag JU, Theunissen CC, Neumann HA. (2002). "Hypertrophic scars after therapy with CO2 laser for treatment of multiple cutaneous neurofibromas". Clinical Orthopaedics and Related Research. 28 (3): 296–8. doi:10.1046/j.1524-4725.2002.01145.x. PMID 11896787.
  2. Packer RJ, Gutmann DH, Rubenstein A, et al. (May 2002). "Plexiform neurofibromas in NF1: toward biologic-based therapy". Neurology. 58 (10): 1461–70. doi:10.1212/wnl.58.10.1461. PMID 12041525.
  3. Isler MH, Fogaça MF, Mankin HJ. (1996). "Radiation induced malignant schwannoma arising in a neurofibroma". Clinical Orthopaedics and Related Research. 325 (325): 251–5. doi:10.1097/00003086-199604000-00031. PMID 8998885.
  4. Namazi H. (2008). "ACE inhibitors: a novel treatment for neurofibroma". Clinical Orthopaedics and Related Research. 15 (5): 1538–9. doi:10.1245/s10434-007-9737-5. PMID 18157575.


Template:WikiDoc Sources