Regístrese
Buscar en
Neurología (English Edition)
Toda la web
Inicio Neurología (English Edition) Unilateral ptosis as the initial sign of multiple myeloma
Journal Information
Vol. 31. Issue 4.
Pages 215-288 (May 2016)
Vol. 31. Issue 4.
Pages 215-288 (May 2016)
Letter to the Editor
DOI: 10.1016/j.nrleng.2014.08.004
Full text access
Unilateral ptosis as the initial sign of multiple myeloma
Ptosis palpebral unilateral como debut de mieloma múltiple
Visits
1134
B. Narberhausa,
Corresponding author
19345bnd@comb.cat

Corresponding author.
, M. Avilab, J. Orriolsc, J. Sauraa
a Servicio de Neurología, Hospital Sant Joan de Déu, Fundació Althaia, Manresa, Barcelona, Spain
b Medicina Familiar y Comunitaria, Area Básica de Salud Manresa 4, Manresa, Barcelona, Spain
c Servicio de Hematología, Hospital Sant Joan de Déu, Fundació Althaia, Manresa, Barcelona, Spain
This item has received
1134
Visits
Article information
Full Text
Bibliography
Download PDF
Statistics
Full Text

Multiple myeloma is the third most frequent haematologic neoplasia, after non-Hodgkin lymphoma and chronic lymphocytic leukaemia. It is characterised by the uncontrolled proliferation of plasma cells in the bone marrow leading to the overproduction of monoclonal immunoglobulins.1

It has an incidence of 5.5 cases/100000 person-years2 and is slightly more frequent in men (male/female ratio, 1.6:1). Mean age of onset is 68 years1; presentation in patients younger than 40 is rare.3

Bone pain, the most frequent symptom of the disease, is present in at least 70% of cases. Patients with myeloma may also present anaemia due to tumour invasion of the bone marrow, hypercalcaemia secondary to bone destruction, renal failure caused by immunoglobulin deposition, and a predisposition to bacterial infections, especially pneumonia or pyelonephritis.1,4

Orbital involvement is rare in multiple myeloma. We present a case of multiple myeloma with an unusual clinical onset of isolated ptosis.

Clinical case

Our patient was a 73-year-old woman with no relevant medical history, who was transferred to our neurology department from the ophthalmology department due to a 3-week history of left-sided ptosis. The ptosis had developed suddenly and did not fluctuate. A few days after our patient first noticed the ptosis, she began to experience occasional episodes of diplopia lasting for several minutes. She reported no bone pain or constitutional symptoms. Physical examination revealed 6-mm left-sided ptosis; no exophthalmos or impaired extraocular movements were seen. Fundus examination revealed no abnormalities.

The neurological examination and general physical examination also showed normal results.

A cranial MRI scan and a CT scan of the paranasal sinuses revealed a lytic lesion on the left orbital floor associated with a soft tissue mass extending to the maxillary sinus and affecting the bony wall of the left nasal cavity. Furthermore, another lytic lesion was found on the right mandibular ramus. A PET scan showed infiltration of the left maxillary sinus, left humerus, and some ribs. Results from the orbital mass biopsy were compatible with plasmacytoma (CD138+, MUM1+, intense positivity for CD56), although lymphoplasmacytic lymphoma could not be ruled out due to the location of the mass. Blood tests revealed mild pancytopaenia, hypogammaglobulinaemia, and the presence of a monoclonal component (0.24g/dL). Immunoelectrophoresis showed a gamma band compatible with IgG-kappa, while a urine test found free kappa light chains. In view of these findings, we decided to perform a bone marrow biopsy, which confirmed the diagnosis of multiple myeloma with plasma cell infiltration (30%).

Discussion

Very few patients with multiple myeloma present neurological symptoms. However, given the characteristics of this entity, there is a wide range of neurological clinical syndromes which may be present during disease progression or even very occasionally representing some of the initial symptoms. Manifestations will depend on the location and size of the tumour.1,3,5 Compression fractures may cause spinal cord compression and/or radiculopathy. Diffuse infiltration of the subarachnoid space (myelomatous meningitis) may also occur. Hypercalcaemia can present with symptoms of encephalopathy. Tumour expansion from facial or cranial bone structures can lead to the involvement of cranial nerves or intracerebral space-occupying lesions. Lastly, amyloid deposition on peripheral nerves can cause mono or polyneuropathy.1

Orbital involvement is rare in the context of multiple myeloma, with very few cases published in the literature. In 2009, Burkat et al.4 conducted a literature review and found a total of 71 cases. In only a third of these were orbital symptoms the initial manifestation of the disease; in the remaining cases, orbital involvement occurred after diagnosis of multiple myeloma.

Myelomas can affect any intraorbital structure. Globes are rarely affected; the most frequent manifestations include retinal haemorrhages, macular detachment, cotton-wool spots, and crystal or copper deposition in the cornea.4

Orbital multiple myeloma normally presents as a solitary soft-tissue tumour originating from bone deposits and is frequently associated with bone destruction.5 According to the literature, involvement is predominantly unilateral (88%); masses are more frequently located in the posterior part of the orbital cavity (69%), and up to 90% of lesions are located in the extraconal space.4

The most frequent initial symptom is exophthalmos (81%) followed by loss of vision (23%), diplopia (23%), palpebral oedema (21%), and ptosis to a lesser extent (13%).4 These data confirm the rareness of our case, which manifested with isolated unilateral ptosis. According to most authors, symptoms begin insidiously.3,6,7

The presence of isolated unilateral ptosis allowed us to rule out oculomotor nerve nucleus or fascicle involvement as a possible cause. Consequently, ptosis could only be due to a dysfunction of either the levator palpebrae superioris muscle or the superior branch of cranial nerve III, which emerges from the posterior part of the orbit.

Neuroimaging results, which show a tumour on the orbital floor, do not reveal direct compression on either of these structures. We hypothesise that the tumour mass may have displaced the orbital contents rostrally, compressing the levator palpabrae superioris muscle against the roof of the orbit.

In our case, myeloma was an IgG secretor, as is the case in the majority of myelomas involving the orbit, to an even greater extent than myelomas in other areas.6

Orbital involvement in myeloma tends to signify a more aggressive form of the disease, and survival rates are significantly poorer in these cases.4

Although fewer than 1% of all orbital tumours are myelomas,1 this possibility should be considered in the differential diagnosis. Careful communication and coordinated teamwork among the different services implicated (in our case, the departments of neurology, ophthamology, otorhinolaryngology, and haematology) are crucial to reach an accurate diagnosis when myeloma presents in this location.

References
[1]
A.S. Fauci, E. Braunwald, D.L. Kasper.
Principios de Medicina Interna.
17a ed., Mc-Graw Hill Interamericana Editores, (2009),
[2]
R. Rodríguez Gil, J.L. Delgado Miranda, B.A. Acosta Acosta.
Tumoración orbitaria como debut de un mieloma múltiple secretor de inmunoglobulina A. A propósito de un caso.
Arch Soc Canar Oftal, (2010), pp. 21
[3]
A. Sharma, M. Kaushal, N.K. Chaturvedi, R. Yadav.
Cytodiagnosis of multiple myeloma presenting as orbital involvement: a case report.
CytoJournal, 10 (2006), pp. 3-19
[4]
C.N. Burkat, J.J. Van Buren, M.J. Lucarelli.
Characteristics of orbital multiple myeloma: a case report and literature review.
Surv Ophthalmol, 54 (2009), pp. 697
[5]
T.V. Ajithkumar, C. Sivasankar, K. Ramachandran.
Orbital multiple myeloma: case report and review of computed tomography features.
Australas Radiol, 46 (2002), pp. 119-120
[6]
F. Thoumazet, A. Donnio, L. Ayeboua, A. Brebion, A. Diedhou, H. Merle.
Orbital and muscle involvement in multiple myeloma.
Can J Ophthalmol, 41 (2006), pp. 733-736
[7]
M. Castro-Rebollo, R. Cañones-Zafra, E.N. Vleming-Pinilla, P. Drake-Rodríguez-Casanova, C. Pérez-Rico.
Exoftalmos unilateral como debut de mieloma múltiple no secretor.
Arch Soc Esp Oftalmol, 84 (2009), pp. 631-634

Please cite this article as: Narberhaus B, Avila M, Orriols J, Saura J. Ptosis palpebral unilateral como debut de mieloma múltiple. Neurología. 2016;31:282–283.

Copyright © 2014. Sociedad Española de Neurología
Article options
Tools
es en pt

¿Es usted profesional sanitario apto para prescribir o dispensar medicamentos?

Are you a health professional able to prescribe or dispense drugs?

Você é um profissional de saúde habilitado a prescrever ou dispensar medicamentos

es en pt
Política de cookies Cookies policy Política de cookies
Utilizamos cookies propias y de terceros para mejorar nuestros servicios y mostrarle publicidad relacionada con sus preferencias mediante el análisis de sus hábitos de navegación. Si continua navegando, consideramos que acepta su uso. Puede cambiar la configuración u obtener más información aquí. To improve our services and products, we use "cookies" (own or third parties authorized) to show advertising related to client preferences through the analyses of navigation customer behavior. Continuing navigation will be considered as acceptance of this use. You can change the settings or obtain more information by clicking here. Utilizamos cookies próprios e de terceiros para melhorar nossos serviços e mostrar publicidade relacionada às suas preferências, analisando seus hábitos de navegação. Se continuar a navegar, consideramos que aceita o seu uso. Você pode alterar a configuração ou obter mais informações aqui.