J Med Cases
Journal of Medical Cases, ISSN 1923-4155 print, 1923-4163 online, Open Access
Article copyright, the authors; Journal compilation copyright, J Med Cases and Elmer Press Inc
Journal website http://www.journalmc.org

Case Report

Volume 5, Number 2, February 2014, pages 62-65


The Association of Leprosy and Spinal Psammomatous Meningioma: A Case Report

Ibrahim Burak Atcia, c, Serdal Albayraka, Necati Uclerb, Emre Durdaga, Omer Aydena

aDepartment of Neurosurgery, Elazig Training Research Hospital, Hospital Street Rizaiye Road, 23100 Elazig, Turkey
bDepartment of Neurosurgery, Adiyaman University, Education and Research Hospital, 02200 Adiyaman, Turkey
cCorresponding author: Ibrahim Burak Atci, Department of Neurosurgery, Elazig Training and Research Hospital, Elazig Training and Research Hospital, Hospital Street Rizaiye Road, 23100 Elazig, Turkey

Manuscript accepted for publication October 2, 2013
Short title: Spinal Psammomatous Meningioma
doi: https://doi.org/10.14740/jmc1389w

Abstract▴Top 

Leprosy or Hansen’s disease (HS) caused by Mycobacterium leprae may involve all organ systems, especially skin and nervous system, and is an contagious disease. The responsible organism is M. leprae which is an acid-fast staining bacilli and similar to M. tuberculosis. Spinal masses are rarely seen tumoral lesions. Intradural spinal masses are generally extradural located meningiomas, nerve-sheath tumors and metastasis. A 68-year-old female patient followed up by a local leprosy center was admitted for new onset lower extremity motor deficits and urinary incontinence. Cervical MRI showed the mass in size of 3 × 1.5 cm. The case was operated under general anesthesia and the lesion was located in the intradural extramedullary space with smooth border and removed totally. The pathologic result was reported as psammomatous meningioma. The purpose of this study was to present the improvement of paraparesis in the case with rarely seen lepromatous type leprosy and a spinal mass which was histologically psammomatous meningioma after emergent surgical intervention.

Keywords: Leprosy; Spinal tumor; Psammomatous menengioma

Introduction▴Top 

Leprosy or Hansen’s disease (HS) caused by Mycobacterium leprae may involve all organ systems, especially skin and nervous system, and is an contagious disease. The responsible organism is M. leprae which is an acid-fast staining bacilli and similar to M. tuberculosis. The bacteria multiply very slowly, and its incubation period is approximately 5 years. Sometimes its symptoms may seen in 25 years. Lepromatous type leprosy, tuberculoid type leprosy, borderline type leprosy and indeterminate type leprosy are four types of leprosy [1]. When we screened the literature, there was no association with leprosy and the common tumors in the literature [2, 3].

Spinal masses are rarely seen tumoral lesions. However, these lesions are the main cause of morbidity, such as extremity dysfunction, urinary and stool incontinance and may lead to mortality associated with these morbidities. Intradural spinal masses are generally extradural located meningiomas, nerve-sheath tumors and metastasis [1]. Meningiomas are mostly seen in older age groups between 5th and 6th decades. Seventy percent of cases with meningioma is female and these tumors are generally located in the thoracal region [1]. Spinal meningiomas are mainly in meningothelial type (29-59%) or psammomatous type (21-57%) [4, 5].

The purpose of this study was to present the improvement of paraparesis in the case with rarely seen lepromatous type leprosy and a spinal mass which was histologically psammomatous meningioma after emergent surgical intervention.

Case Report▴Top 

A 68-year-old female patient followed up by a local leprosy center was admitted for new onset lower extremity motor deficits and urinary incontinence. The patient was suffering from lepromatous type leprosy for 25 years and had advanced lower motor deficits and urinary incontinence. The patient was screened by cranial, cervical and thoracal magnetic resonance imaging (MRI). Cervical MRI showed the mass in size of 3 × 1.5 cm which was peripherally contrasted hyperintense at T-1 weighted MRI sequences (Fig. 1) and hyporintense at T-2 weighted MRI sequences (Fig. 2-4). The case was operated under general anesthesia and the lesion was located in the intradural extramedullary space with smooth border and removed totally (Fig. 5, 6). The pathologic result was reported as psammomatous meningioma (Fig. 7, 8). The patient’s paresis improved after emergent surgical intervention.

Figure 1.
Click for large image
Figure 1. Cervical T-1 weighted MRI.

Figure 2.
Click for large image
Figure 2. Cervical T-2 weighted sagittal MRI .

Figure 3.
Click for large image
Figure 3. Cervical T-2 weighted sagittal MRI sequences.

Figure 4.
Click for large image
Figure 4. Cervical T-2 weighted axial MRI.

Figure 5.
Click for large image
Figure 5. Postoperative T1 cervical sagittal MRI.

Figure 6.
Click for large image
Figure 6. Postoperative T2 cervical sagittal MRI.

Figure 7.
Click for large image
Figure 7. Pathologic result.

Figure 8.
Click for large image
Figure 8. Pathologic result.
Discussion▴Top 

Meningiomas located at spine account for 14-25% of all spinal tumors [6, 7]. The frequency of meningiomas located at spine varies between 1.2 and 12% [8]. These pathologies are commonly located in the thoracal region [9, 10]. Meningiomas are seen 1.5-3 times more common in females than males [9, 10]. Although meningiomas may be seen in all age groups, generelly their frequency increases with age [11].

Spinal meningiomas may show various clinical sypmtoms. Its main sypmtoms are pain, sensory deficits, motor deficits, sphincter deficiency, reflex defects (hyperreflexia and pathologic reflexes) and spasity. Because they are generally slow growing tumors, their sypmtoms emerge slowly rather than acute onset [12].

There is a special classification for the evaluation of patients with spinal meningiomas. McCormick classification or other functional neurologic classifications have been used for spinal meningiomas [6, 13].

The best radiologic modality for spinal meningiomas is spinal MRI. They are seen as isointense at T-1 weighted and T-2 weighted MRI sequences. Sometimes they may be seen hypointense at T-1 weighted MRI and hyperintense at T-2 weighted MRI. These masses are homogeneously contrasted in MRI.

The timing of surgical treatment varies according to patient’s clinical picture as emergent or elective intervention. Meningiomas’ surgery is planned according to tumor localization and size, and generally tumors localized in posterior or postero-lateral part of the spinal canal can be removed with posterior approach by hemilaminectomy, laminectomy or costatransversectomy. Simpson’s intracranial meningiomas classification can be used for surgical resection classification of the spinal meningiomas [14].

It was reported that the surgical resection of psammomatous type among the spinal meningiomas was more difficult and neurologic deterioration after the surgery could be present [14].

When looked at retrospective series in literature, its recurrence rate varies between 1 and 15% [6, 10]. The recurrence is seen generally in high grade meningiomas (grade III-IV). It was reported that the need of re-operation was 22.5% in younger age groups and 10% in older age groups for recurrent spinal meningiomas after total or partial removal of meningiomas [3]. When 80 patients with spinal meningiomas treated surgically are histopathologically examined, it was reported that 87.5% in grade I (meningothelial (57.4%), psammomatous (8.8%), microcystic (1.3%), chordoid (1.3%), fibrous (2.5%)), 7.5% in grade II (atypic), 2.5% in grade III (malign) and 2.5% in grade IV (meningiosarcoma) [12, 15].

Leprosy is a chronic infection caused by the leprosy bacilli firstly found by Armauer Hansen in 1876. Leprosy, known as HS, primarily affects peripheric nerves and secondarily affects skin and other organs and it is progressive disease caused by M. leprae and female/male ratio is about 1:2. Leprosy is mainly a peripheric neuropathy. When the leprosy bacilli invades the body, and then its target is to localize in Schwann cells of the peripheric nerves and its frequency is about 1/10,000 in these cells [2, 3].

The association of leprosy and meningioma has not been reported in literature. In our study, we aimed to present that the development of paraparesia due to psammomatous meningioma in the case with rarely seen lepromatous type leprosy improved after the emergent surgical treatment.


References▴Top 
  1. Van Goethem JW, van den Hauwe L, Ozsarlak O, De Schepper AM, Parizel PM. Spinal tumors. Eur J Radiol. 2004;50(2):159-176.
    doi pubmed
  2. Ferri. Ferri’s Clinical Advisor. 1st ed. 2013.
  3. Bope and Kellerman. Conn’s Current Therapy. 1st ed. 2012.
  4. Levy WJ Jr, Bay J, Dohn D. Spinal cord meningioma. J Neurosurg. 1982;57(6):804-812.
    doi pubmed
  5. Roux FX, Nataf F, Pinaudeau M, Borne G, Devaux B, Meder JF. Intraspinal meningiomas: review of 54 cases with discussion of poor prognosis factors and modern therapeutic management. Surg Neurol. 1996;46(5):458-463, discussion 463-454.
  6. Stanton CA, Challa VR. Meningiomas: pathology. In: Wilkins RH, Rengachary SS, eds. Neurosurgery: Second ed. New York: McGraw-Hill Publisher. 1996:843.
  7. Wen-qing H, Shi-ju Z, Qing-sheng T, Jian-qing H, Yu-xia L, Qing-zhong X, Zi-jun L, et al. Statistical analysis of central nervous system tumors in China. J Neurosurg. 1982;56(4):555-564.
    doi pubmed
  8. Greenberg MS. Handbook of Neurosurgery. Third ed. Florida: Greenberg Graphics. 1994;620-623.
  9. Torres LF, Madalozzo LE, Werner B, de Noronha L, Jacob GV, Medeiros BC, Vialle EN. [Meningiomas. Epidemiological and anatomopathological study of 340 cases]. Arq Neuropsiquiatr. 1996;54(4):549-556.
    doi pubmed
  10. Rohringer M, Sutherland GR, Louw DF, Sima AA. Incidence and clinicopathological features of meningioma. J Neurosurg. 1989;71(5 Pt 1):665-672.
    doi pubmed
  11. Kuratsu J, Takeshima H, Ushio Y. Trends in the incidence of primary intracranial tumors in Kumamoto, Japan. Int J Clin Oncol. 2001;6(4):183-191.
    pubmed
  12. Das A, Tang WY, Smith DR. Meningiomas in Singapore: demographic and biological characteristics. J Neurooncol. 2000;47(2):153-160.
    doi pubmed
  13. Yurt A, Kocanogulları O, Cakir Y, Bardakci S ve ark. Spinal meningiomlar. Ege Tip Derg. 1999;38(3):145-148.
  14. Cordera S, Bottacchi E, D'Alessandro G, Machado D, De Gonda F, Corso G. Epidemiology of primary intracranial tumours in NW Italy, a population based study: stable incidence in the last two decades. J Neurol. 2002;249(3):281-284.
    doi pubmed
  15. Gezen F, Kahraman S, Canakci Z, Beduk A. Review of 36 cases of spinal cord meningioma. Spine (Phila Pa 1976). 2000;25(6):727-731.
    doi


This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


Journal of Medical Cases is published by Elmer Press Inc.

 

Browse  Journals  

 

Journal of Clinical Medicine Research

Journal of Endocrinology and Metabolism

Journal of Clinical Gynecology and Obstetrics

 

World Journal of Oncology

Gastroenterology Research

Journal of Hematology

 

Journal of Medical Cases

Journal of Current Surgery

Clinical Infection and Immunity

 

Cardiology Research

World Journal of Nephrology and Urology

Cellular and Molecular Medicine Research

 

Journal of Neurology Research

International Journal of Clinical Pediatrics

 

 
       
 

Journal of Medical Cases, monthly, ISSN 1923-4155 (print), 1923-4163 (online), published by Elmer Press Inc.                     
The content of this site is intended for health care professionals.
This is an open-access journal distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License, which permits unrestricted
non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Creative Commons Attribution license (Attribution-NonCommercial 4.0 International CC-BY-NC 4.0)


This journal follows the International Committee of Medical Journal Editors (ICMJE) recommendations for manuscripts submitted to biomedical journals,
the Committee on Publication Ethics (COPE) guidelines, and the Principles of Transparency and Best Practice in Scholarly Publishing.

website: www.journalmc.org   editorial contact: editor@journalmc.org
Address: 9225 Leslie Street, Suite 201, Richmond Hill, Ontario, L4B 3H6, Canada

© Elmer Press Inc. All Rights Reserved.


Disclaimer: The views and opinions expressed in the published articles are those of the authors and do not necessarily reflect the views or opinions of the editors and Elmer Press Inc. This website is provided for medical research and informational purposes only and does not constitute any medical advice or professional services. The information provided in this journal should not be used for diagnosis and treatment, those seeking medical advice should always consult with a licensed physician.