Literature DB >> 35341222

Syringomyelia Managed with Classical Homeopathy: A Case Report.

Elena Rudakova1, Seema Mahesh2, George Vithoulkas3,4.   

Abstract

Syringomyelia (SM) with Chiari malformation is a rare disease with an unpredictable course. Surgery and other interventions help reduce the severity of symptoms, but over 50% patients require re-operation. Auto-resolution is rare in this type of SM, and most cases progress to complications, which may amount to a great burden. The patient of SM with Arnold-Chiari malformation type 1 in a 54-year-old Russian woman who was treated with individualized classical homeopathy for over eight years with remarkable improvement in the clinical signs and symptoms of the condition and comorbidities. On MRI, the syrinx completely resolved, which further confirmed the benefit of this therapy. This case of SM with Arnold-Chiari malformation type 1 seemed to benefit from individualized classical homeopathy. Scientific investigation into an individualized classical homeopathic approach towards SM is necessary to establish its relevance in this condition.
© 2021 Indian Academy of Neurosciences (IAN).

Entities:  

Keywords:  Arnold-Chiari malformation; Homeopathy; Syringomyelia

Year:  2021        PMID: 35341222      PMCID: PMC8948329          DOI: 10.1177/09727531211046370

Source DB:  PubMed          Journal:  Ann Neurosci        ISSN: 0972-7531


Introduction

Syringomyelia (SM) is a rare, progressive disease of the spinal cord and it presents with mild to severe neurological complaints, with the characteristic intramedullary cyst,1 occurring mostly from underlying causes such as Chiari malformations (CMs).1 CM incidence is approximately 3–8/100,000, with 62% to 80% exhibiting SM,2 and it shows a predilection to certain geographic locations such as Russia.34 Over 50% of the cases are because of Arnold-Chiari malformation type 1, characterized by herniation of cerebellar tonsils through the foramen magnum, followed by trauma-related incidence (25% of cases), the other types being rarer.15 Many theories were proposed to explain the dynamics behind the development of SM, including the three popular theories of Gardner, Williams, and Oldfield.1 The common vein running through these theories is a disturbance in the circulation of cerebrospinal fluid (CSF), resulting from an aberrant resorption, or a mechanical block to circulation, or disorder of spinal cord mobility.1 SM is classified into communicating, noncommunicating, atrophic, and neoplastic types. This classification helps decide whether shunting, surgery, or conservative treatment is the best option.6 The understanding of SM pathophysiology remains patchy, which makes its diagnosis and treatment a challenge.7 The diagnosis of SM is made by the appreciation of the fluid-filled cavity in the spinal cord related to CSF circulation disturbance, cord tethering, or an intramedullary tumour.7 The symptoms result from herniation of cerebellar tonsils or the compression of nerves. The most common symptoms in SM with CM are headache, dizziness, insomnia, weakness in the upper extremities, neck pain, numbness and tingling in the extremities, and other neurological symptoms.8 The severity depends on the size and duration of the syrinx. Rapidly progressing cases show more severe symptoms than cases that progress slowly over many years.4 Management is conservative when neurological symptoms are absent or mild. However, most patients exhibit disease progression with conservative treatment.1 When the symptoms are severe, surgery/shunting/cordectomy/cellular neuro-construction may be offered to the patient, depending on the underlying cause.1 Stabilization of the neurological symptoms and improvement in the general condition are the aims of treatment.2 Surgery is effective in most cases, but over 50% of patients require re-operation at some point.1 Auto-resolution of SM is rarely reported, and sometimes the auto-resolution is not associated with any difference in clinical symptoms.9 We present a rare case of SM with Arnold Chiari malformation type 1 that progressed considerably until the application of classical homeopathic treatment, and regressed under this therapy over the years. A benefit was also seen in the comorbidities. The literature did not yield any other similar case where SM benefited from homeopathy.

Case Presentation

The patient, a Russian woman, medical doctor (ultrasonologist), was 54 years old when she presented for a homeopathic consultation in June 2012. The diagnosis was made in 2006 using an MRI, but she was not given any medication or therapy.

Presenting Complaints

The patient had severe neurological complaints at the time of homeopathic consultation, including pain, burning, and tingling in the dorsum of hands; sharp pains in the first metacarpophalangeal joints; and coldness of the hands. She dropped things suddenly and could not feel how they fell out of her hands. There was pain under the right scapula, in the lumbar and sacral regions, and in her feet. She experienced incontinence of urine when laughing or coughing and reported a pulsating noise in the head.

Other Complaints

Other complaints include deep bleeding cracks in the patient’s fingertips every winter; flushes of heat, disturbing her sleep; dryness in the vagina; epigastric and umbilical region pain with bloated feeling; and deep acne on the face.

History of Presenting Complaints

In 1995, the patient developed vertigo and pain in the hands. She also developed tingling and burning in linear areas in the upper arms, forearms, and dorsum of the hands. Pain in the first her metacarpophalangeal joints increased so much that sometimes she was unable to move the ultrasound probe. She started dropping things suddenly with insensibility. An MRI in 2006 led to the diagnosis of SM. The neurologist told her to avoid activities such as lifting weights and abdominal crunches, but no therapy/medication was given. She stopped visiting a chiropractor. Follow-up MRIs were performed occasionally.

Past Medical History

The patient suffered hepatitis at the age of three years, had recurrent tonsillitis and occasional gastric pains in childhood, and later developed recurrent tracheitis with high fevers, which continued to occur at intervals at the time of consultation. She was treated mostly with antibiotics for these infections. At 20 years of age, a gastroscopy revealed no gastritis but an increased motility of the stomach. At the age of 46 years, she was treated with lithotripsy for left renal colic. At 52, she had pneumonia and was given antibiotics. She still suffered occasional flu with high fever. She had pain in the sacral region since she was 34 years old and was visiting a chiropractor for this issue. She had acne since puberty.

Obstetrics and Gynecological History

The patient attained menarche at the age of 13 years. She had two children without event. She underwent electrocoagulation for erosion of cervix at the age of 22 years and laser treatment for leukoplakia of cervix at 45 years. Since April 2011, she had menopausal symptoms, and a cytological examination of the vagina showed atrophy of the mucosa. She applied estrogen cream as recommended by the gynecologist but stopped doing it as she developed swelling in the breasts.

Family History

The patient’s father had hypertension and died from rupture of abdominal aortic aneurism at the age of 82 years. Her mother had brain stroke at the age of 65 years, hypertension and vascular dementia. She died at the age of 76 years.

Diagnosis

The patient was diagnosed as having SM with Arnold-Chiari malformation type 1 (ICD10: G95.0).10

MRI: Cervical and Upper Thoracic Spine on February 15, 2006 (Figure 1)

There is a hydromyelic cavity in the spinal cord extending from the level of C3 to T1 vertebra. The maximum diameter of the cavity is 5 mm. The spinal cord below this level has normal diameter and structure. The vertebral body height is normal, and there are no focal lesions. There is straightening of cervical lordosis with formation of pathological kyphosis. There is decreased intensity of signal from the intervertebral discs of the cervical spine (evidence of dehydration). There are dorsal central disc protrusions, up to 3 mm in size, with mild intervertebral foraminal narrowing at the levels of C4–C5 and C5–C6. There is circumferential disc hernia (4 mm dorsally) with signs of intervertebral foraminal narrowing on both sides (mostly right) at the C6–C7 level. There is descent of cerebellar tonsils below the foramen magnum (an MRI of the brain is recommended). Hydromyelia at the level of C3–T1. Osteochondrosis of the cervical and upper thoracic spine. Disc hernia at C6–C7.

MRI: Brain and Intracranial Arteries on March 15, 2006

Midline structures are not displaced. The size of the ventricles is normal. There is mild asymmetry of the lateral ventricles (Sinister > Dexter). There are no focal lesions in the brain. Subarachnoid spaces are not widened. The size of the hypophysis is normal. The stem structures are within normal limits. The cerebellar tonsils extend 5 mm below the Chamberlain line. The paranasal sinuses are filled with air. MR angiography of the intracranial arteries did not show any evidence of occlusion or aneurism of arteriovenous malformations. There are no focal lesions in the brain matter. A repeat MRI in July 2008 showed progression of the disease.

MRI: Brain and Cervical Spine on July 22, 2008

The MRI of the brain shows a single, small (up to 3 mm) hyperintense lesion in the white matter of the left frontal lobe near the anterior horn of the lateral ventricle. A second small lesion is at the border between cortex and white matter in the left cerebellar hemisphere. No other space-occupying lesions or sites of pathological MR-signal are identified. There is widening of perivascular Virchow-Robin spaces. Midline structures are not displaced. The ventricles are of normal position, shape, and size. The lateral ventricles are asymmetrical (Sinister > Dexter). The basal cisterns are normal. The external subarachnoid space is uneven in width along the convex surface of the cerebral hemisphere; it is slightly dilated in the frontal-parietal areas and normal in other areas. There is ectopia of cerebellar tonsils, not more than 6 mm to the posterior parts of the foramen magnum. The paranasal sinuses are filled with air. MR angiography of the brain vessels shows no pathological tortuosity, deformities, or dilatations of the arteries, and the vessel lumens are homogenous.

Arnold-Chiari Malformation Type I.

Signs of Vascular Encephalopathy

MRI of the cervical spine showed that the syringomyelial cyst found in previous investigations is now extending from the level of C3 to the upper part of the T3 vertebral body. The shape and structure of the cyst (consisting of several confluent cysts with septa) are the same as a previous investigation on December 5, 2006. The maximum diameter is up to 7 mm at the level of the C7 vertebra. The contour of the cyst at the border with the normal part of the spinal cord is “sharp” – a variant of a cavity with low pressure. The haemangioma at the posterior part of the C7 vertebra is the same in size and shape. Signs of osteochondrosis at the level of C4–C7 vertebrae with maximal pathological changes (posterior disc hernia) at the level of C6–C7 vertebrae. SM at the level of C3–T3 vertebrae. Osteochondrosis of the cervical spine. Haemangioma of C7 vertebra.

Differential Diagnosis

SM may be confused with neuropathic disorders, such as diabetic neuropathy, and other more common neurological disorders, such as Guillain-Barré syndrome, amyotrophic lateral sclerosis, and multiple sclerosis.11 The diagnosis was confirmed on an MRI of the brain and spinal cord.

Homeopathic Consultation

The patient sought a homeopathic consultation on June 24, 2012. Her neurological symptoms had escalated to the list mentioned earlier. She also had menopausal symptoms and dermatitis. Homeopathic prescriptions consider the totality of symptoms and not just those of SM. This extends to the patient’s mental/emotional suffering. A detailed history revealed that she suffered repeated events causing grief in the past. She experienced tremendous fear that something bad would happen to her family and they would die. She dreaded phone calls anticipating bad news. She had sudden episodes of fear, thinking she lost something, such as the keys to her car. She checked and rechecked if she closed the doors and the taps. Note: The bold text indicates significant change. Note: The causality score is high for the treatment in this case, implying that the effects were indeed attributable to homeopathic treatment This specific kind of anxiety and memory loss, along with the history of grief with the physical problems in the nervous system, indicated the homeopathic remedy Causticum hahnemanni (Figure 2).12
Figure 2.

Repertorisation of the Symptoms at Presentation to Homeopathy.

Prescription

Causticum 30 CH, One Dose

The rationale behind prescribing Causticum is that the primary pathology in a patient requiring causticum is prolonged grief, bringing down the immune system. A patient in such a condition exhibits absentmindedness and nervousness. Causticum also has this symptom of having extreme intolerance to injustice from being sympathetic. Further, the cracking of skin and coldness of hands are a part of its proving. The symptom of involuntary urination on coughing is a hallmark of causticum monograph.

Follow Up

After the remedy, pain in the patient’s hands with tingling and burning sensations increased for a period of time (what is termed “therapeutic aggravation” in homeopathy), but the hands became warmer and she sometimes felt heat in her hands. The flushes of heat increased for a period time. Her energy level became better. Her mood improved, and her anxiety diminished. This case had a long follow up of eight years with constant ups and downs. She received Causticum in different potencies from time to time whenever the symptoms worsened, with good effects most of the time. She also received Causticum for acute episodes, such as trigeminal neuralgia. Few other remedies were given when she had acute inflammatory diseases, such as common cold, acute otitis media, respiratory infection, and intestinal infection. She was given Mercurius solubilis, Arsenicum album, Graphites, Eupatorium perfoliatum, and Gelsimium sempervirens for these. The otitis did not respond to Graphites, and she used antibiotic ear drops and steroids. She experienced multiple traumas and fractures during these eight years, despite there being no obvious deficits in her balance, and was given Rhus toxicodendron, Ruta graveolens, and Arnica montana as required. She also received nonsteroidal anti-inflammatory drugs (NSAIDs) for the traumas. There was once a severe pain in the sacral region that extended to the hip, thigh, and knee. She was then given meloxicam (NSAID) and injections of vitamins B1, B6, and B12. These treatments given interspersed with her main complaints relieved the incidental episodes. However, the mainstay of her treatment was Causticum, and it nearly always relieved her core symptoms. This is typical in a chronic running case with classical homeopathic treatment, that there may arise need for different remedies during the acute diseases but they may need repetition of the same remedy for chronic condition after such episodes for the case to proceed in the right direction. The relapses were progressively milder over the years until they significantly improved at the last follow-up on October 8, 2020. The patient’s report at the last follow-up is detailed further. She stopped dropping things and the pain in her hands reduced. She worked more freely. The tingling, burning, and coldness in the hands were gone, and the deep cracks on the fingers disappeared. The acne was less severe. The anxiety about family was less intense. She did not recheck as frequently. The paresthesia in the calves, which she had experienced since May 2019, had decreased for several days after the last remedy, but relapsed after one week. The dryness in the eyes that had appeared occasionally since March 2014 persisted. The flushes of heat persisted. Sleep remained poor, waking three to four times during the night, but she fell asleep easier. Her acute inflammatory conditions over the years became milder than before her starting homeopathy. When asked to repeat the brain MRI for final analysis, the patient refused because she was severely affected by the procedure and, in her own words, “I am healthy, young and beautiful and I will never ever have to do MRI again.” The changes in the MRI are presented in Figure 3 and Table 1. Notably, the syrinx cavity increased in size from 2006 to 2008, regressed progressively after the commencement of homeopathic treatment, with a complete obliteration of the cavity in the latest MRI of March 2020.
Figure 3.

MRI Films for Comparison From 2008 to 2020.

Table 1.

Changes in MRI From 2008 to 2020

DateMRI BrainMRI Spine
April 23, 2015Small single areas of hyperintense MR-signal located in the subcortical parts of the white matter in frontal-parietal areas and paraventricularly on both sides. The maximum diameter of the lesion is 2.7 mm. In the subcortical area of the right cerebral hemisphere against the dilated perivascular spaces, there are several grouped cysts of different caliber with homogenous content, up to 4 mm in size. There are no perifocal changes around these lesions, and they do not exert a mass effect on the adjacent brain structures. There are no recent ischaemic changes on the diffusion weighted images.The lateral ventricles are asymmetrical, the left lateral ventricle is slightly wider. External subarachnoid space along the cerebral hemispheres is slightly dilated in the frontal-parietal areas and normal in the other areas. There is ectopia of cerebellar tonsils to the posterior parts of foramen magnum not more than 5 mm. The nasal septum is deflected. There is a moderate increase in the number of lesions compared to the investigation on July 22, 2008. Conclusion: MRI picture of Arnold-Chiari malformation type I. Signs of vascular encephalopathy.Marked improvement compared to the investigation on July 22, 2008—an absence of syringomyelia cysts. There is a local dilatation of the central canal at the level of C2 and C3 vertebrae (up to 1.6 mm in anteroposterior dimension, 6.7 mm and 14 mm in length, respectively). The vertebral body height is normal. The MR-signal from their structure is altered because of the degenerative-dystrophic changes with posterior marginal osteophytes. There is a hyperintense MR-signal in the posterior part of C7 vertebra—a haemangioma of the same size and shape. There are lesions with the same signal characteristics in the body of the C6 vertebra (5x3 mm in size) and in the body of C4 vertebra (9x5 mm in size). MR-signal from all the disks is reduced in T2-weighted images. There is a reduction of disc height at the levels of C4–C7 vertebrae. There is a narrowing of the right lateral recess with a compression of the root because of the disc protrusion up to 3 mm and a posterior marginal osteophyte at the level of C6–C7 vertebrae. There is an induration of ligamentum flavum at the level of C6–C7. There is a scoliotic deviation in the longitudinal axis, the cervical lordosis is straightened. The thoracic kyphotic curve is increased. There is a mild wedge-shape deformity of the T7 vertebra. The MR-signal from their structure is altered because of dehydration. Conclusion: A disturbance of statics of the cervical and thoracic spine. Osteochondrosis and spondylosis of the spine with the biggest changes at the level of C6–C7 vertebral segment (with right paramedian disc protrusion and root compression). Hydromyelia at the levels of C2 and C3 vertebrae. There is a marked improvement compared to the investigation on July 22, 2008—the previously visualized syringomyelia cysts at the level of C3–T3 vertebrae are absent.
October 31, 2017The quantity and size of lesions in the subcortical and periventricular white matter of the frontal-parietal areas are the same as the investigation on April 23, 2015. There remains a widening of perivascular Virchow-Robin spaces with a visualization of a cystic dilatation up to 4 mm at the right side. The lateral ventricles remain asymmetrical, the left lateral ventricle is slightly wider. External subarachnoid space along the convex surface of the cerebral hemispheres is uneven in width—it is slightly dilated in the frontal-parietal areas and normal in other areas. There is an ectopia of cerebellar tonsils to the posterior parts of foramen magnum not more than 5 mm as before. Conclusion: MRI picture of Arnold-Chiari malformation type I. Signs of microangiopathy with no negative changes compared to the investigation on April 23, 2015.Persisting dilatation of the central canal at the level of C2 and C3 vertebrae. The length of the dilated part is the same at the level of C2 vertebra (6.7 mm) and is less at the level of C3 vertebra at 6.2 mm (compared to 14 mm at the previous investigation). The haemangioma in the right part of C4 vertebra is 8x5 mm in size, and the haemangioma in the posterior-right part of C7 vertebra is 10x7 mm in size, which is not enlarged compared to the previous investigation, and there is a small lesion in the C6 vertebra. Signs of osteochondrosis at the level of C4–C7 vertebrae with the biggest changes at the level of C6–C7 vertebrae. Uneven disc bulging at the posterior semicircle with a maximum right paramedian bulging up to 3 mm and a narrowing of right intervertebral foramen. Pronounced thoracic kyphotic curve. There is a mild scoliotic deviation in the longitudinal axis. The vertebral body height is normal. The MR-signal from the vertebral bodies is altered because of the degenerative changes. MR-signal from the disks is reduced because of the dehydration. There are no dorsal disc protrusions. Investigation in the myelography mode showed a dilatation of root pouches at the level of T6–T12 vertebrae. Conclusion: Osteochondrosis of the cervical and thoracic spine with the biggest changes at the level of C6–C7 vertebral segment (posterior right paramedian disc protrusion). Hydromyelia at the level of C2 and C3 vertebrae. Haemangiomas in C4, C6, and C7 vertebral bodies. A disturbance of statics of the spine. There are no negative changes compared to the investigation on April 23, 2015.
March 25, 2020Not performedAt the level of C2 vertebra, the central canal of the spinal cord is visualized up to 1 mm in width at the length of 6 mm. The central canal in all other parts of the cervical and thoracic region is not dilated. There are no cysts in the spinal cord. The vertebral body height is normal. The vertebral body contours are deformed because of the osteophytes (the anterior marginal osteophytes in the middle thoracic spine are most prominent). The intensity of signal from the vertebral bodies is heterogenous because of the degenerative changes in the marrow. There are areas of accumulation of fatty tissue (hypointense in the STIR mode) in the C4, C7, and T6 vertebral bodies. There is a decreased intensity of signal from the intervertebral discs of the cervical and thoracic spine in because of dehydration. There are dorsal disc protrusions on a wide base at the levels of C6–C7 (3.5 mm), C4–C5, C5–C6 (up to 3 mm), causing moderate intervertebral foraminal narrowing. There is a moderate hypertrophy of the ligament flava at the level of C6–C7, leading to deformity of the dural sac in the dorsal part. Conclusion: There are no focal lesions, cysts, or any significant widening of the central canal of the spinal cord. Osteochondrosis or spondyloarthrosis of the cervical and thoracic spine.

Note: The bold text indicates significant change.

Discussion

In this case of SM with CM type 1, classical individualized homeopathy was beneficial—as appreciated on the MRI—and complete resolution of the syrinx was evident. The clinical signs and symptoms of SM improved along with the crippling anxiety that she suffered. There was also remarkable improvement in her memory, dermatitis, and acne. The frequent infections with high fever also became milder after the treatment. The causality score on modified Naranjo criteria for assessing causal attribution of clinical outcome to homeopathic intervention was 12 (Table 2).
Table 2.

Modified Naranjo Criteria for Assessing Causal Attribution of Clinical Outcome to Homeopathic Intervention

Criteria Y N Not Sure/NA Case
1. Was there an improvement in the main symptom or condition for which the homeopathic medicine was prescribed?2-102
2. Did the clinical improvement occur within a plausible time frame relative to the drug intake?1-201
3. Was there an initial aggravation of symptoms?1001
4. Did the effect encompass more than the main symptom or condition, that is, were other symptoms ultimately improved or changed?1001
5. Did the overall well-being improve?1001
6 (A) Direction of cure: did some symptoms improve in the opposite order of the development of symptoms of the disease?1000
6 (B) Direction of cure: Did at least two of the following aspects apply to the order of improvement of symptoms: from organs of more importance to those of less importance, from deeper to more superficial aspects of the individual, and from the top downwards1001
7. Did “old symptoms” (defined as nonseasonal and noncyclical symptoms that were previously thought to have resolved) reappear temporarily during the course of the improvement?1001
8. Are there alternate causes (other than the medicine) that with a high probability could have caused the improvement? (consider known course of disease, other forms of treatment, and other clinically relevant interventions)-3101
9. Was the health improvement confirmed by any objective evidence? (in this case MRI)2002
10. Did repeat dosing, if conducted, create similar clinical improvement?1001
Total 12

Note: The causality score is high for the treatment in this case, implying that the effects were indeed attributable to homeopathic treatment

The Levels of Health theory13 explains that a patient born with a higher “level of health” generally has a good prognosis despite dire diagnoses. This theory provides tangible methods to categorize a patient’s level of health. Despite having a chronic neurological condition, our patient generated high fevers during acute episodes, an indication that she was of higher health level and good prognosis. Accordingly, deep positive changes were appreciated in the follow-ups, and she proceeded in the right direction according to homeopathic laws (Figure 4). She proceeded from a deeper pathology involving the spinal cord (nervous system) to a predominantly vertebral pathology (musculoskeletal system), namely, from SM to spondyloarthrosis. While this may still continue to disturb the patient and require treatment, the limitation is much more superficial. This effect was demonstrated in other cases with serious pathology, with concomitant ability to induce high fever during acute infections.14 However, such response may not be expected in all cases.
Figure 4.

Direction of Cure as Seen in the MRI Reports.

The homeopathic remedy Causticum hahnemanni is indicated in deep neurological conditions, anxiety, depression, and memory issues.12 Classical homeopathy previously exhibited clinical effects in deep pathologies,14 but the effects of Causticum are limited in the published literature. The limitation here was the inability to demonstrate any pharmacological effect of the remedy because homeopathy does not act on the matter but on the energy fields of the organism,15 a perspective not yet experimentally demonstrated. There is also a remote possibility of auto resolution, as seen in rare cases of SM with CM,9 which was unlikely because our case was on a progressive pathological path at the time of homeopathic consultation.

Conclusion

This case of SM with Arnold-Chiari malformation type I benefited from individualized classical homeopathy, as seen on MRI reports and appreciated in clinical signs and symptoms. There is a need to scientifically investigate the individualized approach to SM cases.
  10 in total

1.  How Should Syringomyelia be Defined and Diagnosed?

Authors:  Jörg Klekamp
Journal:  World Neurosurg       Date:  2018-01-06       Impact factor: 2.104

Review 2.  [Syringosubarachnoid shunting in treatment of syringomyelia: a literature review and a clinical case report].

Authors:  V S Klimov; Yu S Gulay; A V Evsyukov; G I Moysak
Journal:  Zh Vopr Neirokhir Im N N Burdenko       Date:  2017

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Journal:  World Health Stat Q       Date:  1988

4.  Embryonal Carcinoma with Immature Teratoma: A Homeopathic Case Report.

Authors:  Seema Mahesh; Mahesh Mallappa; George Vithoulkas
Journal:  Complement Med Res       Date:  2017-10-30       Impact factor: 1.211

5.  Spontaneous Resolution of Syringomyelia with a 16-Year Serial Magnetic Resonance Imaging Follow-Up: A Case Report and Literature Review.

Authors:  Chenghua Yuan; Qingyu Yao; Can Zhang; Fengzeng Jian
Journal:  World Neurosurg       Date:  2019-07-24       Impact factor: 2.104

6.  Classification of syringomyelia.

Authors:  T H Milhorat
Journal:  Neurosurg Focus       Date:  2000-03-15       Impact factor: 4.047

7.  Syrinx size and duration of symptoms predict the pace of progressive myelopathy: retrospective analysis of 103 unoperated cases with craniocervical junction malformations and syringomyelia.

Authors:  E I Bogdanov; E G Mendelevich
Journal:  Clin Neurol Neurosurg       Date:  2002-05       Impact factor: 1.876

8.  Prospective analysis of presenting symptoms among 265 patients with radiographic evidence of Chiari malformation type I with or without syringomyelia.

Authors:  Diane M Mueller; John J Oro'
Journal:  J Am Acad Nurse Pract       Date:  2004-03

9.  [Results of surgical treatment of syringomyelia associated with Chiari 1 malformation. An analysis of 125 cases].

Authors:  A A Zuev; N V Pedyash; D S Epifanov; G V Kostenko
Journal:  Zh Vopr Neirokhir Im N N Burdenko       Date:  2016
  10 in total

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