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Int Orthop. 2009 June; 33(3): 605–610.
Published online 2008 January 24. doi:  10.1007/s00264-007-0483-x
PMCID: PMC2903125

Language: English | French

Mazabraud’s syndrome: a new case and review of the literature

Abstract

The association between muscular myxomas and fibrous dysplasia is a rare condition known as Mazabraud’s syndrome, as reported by Henschen (Verh Dtsch Ges Pathol 21:93–97, 1926) and Mazabraud A and Girard (Rev Rhum Mal Osteoartic 24(9–10):652–659, 1957). We report a case of a 32-year-old woman with multiple myxomas in her right thigh and monomelic fibrous dysplasia. A review of the international literature referring to 67 cases to date was carried out. The syndrome is characterised by the following features: females are twice as likely to be affected as males; the lower limbs are the most frequently affected, fibrous dysplasia is more common in the femur and the pelvis and myxomas in the quadriceps muscle; myxoma is multiple in more than 70% of cases. Although there has never been any continuity between tumours and bone lesions, a significant correlation between dysplastic bone and myxoma has been revealed.

Résumé

L’association entre un myxome musculaire et une dysplasie fibreuse est rare (Mazabraud, 3 à 6). Nous avons rapporté le cas d’une femme de 32 ans présentant un myxome musculaire multiple, au niveau de la cuisse droite et une atteinte de dysplasie fibreuse. La revue de la littérature internationale permet de rapporter 67 cas caractérisant une telle symptomatologie. Les femmes sont atteintes deux fois plus fréquemment que les hommes et les membres inférieurs également (la dysplasie fibreuse est fréquente au niveau du fémur et du bassin). Le myxome musculaire étant surtout localisé au niveau du quadriceps. Ces myxomes présentent généralement des lésions multiples dans 70% des cas. Si on ne peut pas mettre en évidence de continuité entre ces deux tumeurs, leur association existe néanmoins.

Case report

A 32-year-old Caucasian female presented to the plastic surgery department of a general hospital for the evaluation of a mass present in the medial aspect of the right thigh. The diameter was 8 cm, which had gradually increased in size over the past two years since the patient first noted it. The surgeons decided to excise the lesion which was located in the vastus medialis, of oval shape, dimensions 6.5 × 4.4 × 3.5 cm, with a hard-elastic consistency and traslucid with myxoid appearance after removal.

Another smaller lesion was removed from the same area.

Histological examination showed a tissue with spike- and star-shaped cells in an abundant myxoid matrix; no mitotic activity was documented. Immuno-histochemical results were slightly positive for s100 and negative for CD99, EMA, CD56 and CD57. A diagnosis of myxoma was proposed.

Nuclear magnetic resonance (NMR) imaging, performed post-operatively, revealed the presence of multiple lesions in the femur and right tibia, with low signal intensity on T1-weighted images (Fig. 1) and high signal intensity on fat-suppression sequence images (Fig. 2). Successive X-rays showed evidence of multiple radiodense lesions with smooth margins in the proximal third of the right tibia and right femur, not affecting cortical bone (Figs. 3 and and44).

Fig. 1
Low signal intensity on T1-weighted images
Fig. 2
High signal intensity on fat-suppression sequence images
Fig. 3
Proximal right femur; radiodense lesion with smooth margins
Fig. 4
Right tibia; multiple radiodense lesions with smooth margins

Clinical examination revealed no shortening. No endocrine problems were noted but “café au lait” spots were present on the medial aspect of the right upper limb (Fig. 5).

Fig. 5
“Café au lait” spots on the medial aspect of the right arm

Bone scan showed evidence of increased uptake in the proximal third of the right femur and particularly in the proximal right tibia (Fig. 6).

Fig. 6
Increased uptake in the proximal third of the right femur and right tibia

A diagnosis of Mazabraud’s syndrome was made and the patient was included in a follow-up programme for patients with fibrous dysplasia. No surgical operation was performed.

Materials and methods

Since Henschen [3] first described Mazabraud’s syndrome in 1926, 68 cases, including ours, have been listed to date. These were reviewed. Table Table11 lists the results.

Table 1
Mazabraud’s syndrome cases; the black boxes indicate that further explanation is possible or necessary

Two of these cases were removed from the study because we could not find the original articles or information in other reviews [1, 8].

To validate age onset, a t-test for independent groups was applied and Fisher’s test was used to analyse the distribution of fibrous dysplasia lesions.

Tsitouridis et al. [9] described a case where precocious puberty was considered at 11 years, but in our review, it was considered normal.

The syndrome population is composed of 46 women (67.65%) and 20 men (32.35%).

Results and discussion

Fibrous dysplasia is a non-malignant infrequent condition caused by a mutation in the GNAS gene, located on chromosome 20q13.2–q13.3, encoded to a Gs(α) protein and enrolled in proliferation cell activity. Mutations increase protein activity and abnormal proliferation. Mosaic cell distribution is present, leading to a pathological bone when the mutation is in bone cells and to McCune-Albright syndrome when endocrine cells are affected [2, 10].

Fibrous dysplasia is characterised by the presence of non-ossifying areas in bone. It may be monostotic or polyostotic and is usually unilateral. It can be associated with endocrine disturbance such as precocious sexual development or goitre and diabetes mellitus. There may be “café au lait spots” indicating a condition known as McCune-Albright syndrome. When associated with myxoma, it is known as Mazabraud’s syndrome.

Myxoma is a benign neoplasm usually diagnosed in the sixth to seventh decades of life. It can be single or multiple. In Mazabraud’s syndrome, it is frequently multiple and combined with a dysplastic bone without any continuity between the lesions.

The most important feature is that the myxoma develops 12 years before fibrous dysplasia diagnosis. Females are affected twice as often as males. Fibrous dysplasia is often polyostotic and the femur is the most commonly affected. Myxomas are often multiple and thigh muscles are more frequently involved.

Age, sex and race We knew the onset of fibrous dysplasia in 52 cases. It was usually diagnosed between 1 year to 67 years of age, with an average of 32.42 years (variance 315.03, median 34). In four other case studies, we only knew that it was diagnosed in infancy and in four other cases, diagnosis was achieved before myxoma.In five cases, no information about the onset of the different components are reported.In one case, the age at diagnosis was not available.In 60 cases, we knew the age of myxoma onset, which usually arose between 17 to 82 years of age, with an average of 44.32 years (variance 177.27, median 42).As already mentioned, in five cases, age was not recorded at diagnosis of different syndrome components, whereas in one case, there is no information about myxoma age onset.In 14 cases, fibrous dysplasia had been discovered with myxoma onset; in nine cases, it was noted after and in 29 cases, it was noted before myxoma. On average, myxoma becomes significantly symptomatic 12.06 years after fibrous dysplasia (data from 52 cases, variance 274.92, p < 0.001).Although fibrous dysplasia and myxomas, when isolated, have no sex-related incidence, when associated, women revealed a two-fold greater incidence than men (46 females and 20 males).Although a major incidence in Caucasian people are reported, it is not possible to make any conclusion about race predominance because of the rarity of the syndrome and the high rate of misdiagnosis.

Localisation; in only one case did we have information about lesion localisation In 13 cases, fibrous dysplasia was monostotic (19.70%); in 53 cases, it was polyostotic (80.30%). In 24 cases, fibrous dysplasia was bilateral and in 29 cases, it was unilateral. Unilateral forms were distinguished as follows: 18 right, 10 left and one not specified; 15 were hemimelic and 14 were monostotic.Despite the fact that polyostotic fibrous dysplasia is more frequent in females than in males this difference has a low score of significance (Fischer test, p = 0.51), therefore, the distribution is not sex-related.The distribution of the fibrous dysplasia was recorded in 57 patients and was found to be most frequently located in the femur (47 in the femur, ten only in the femur and 25 in the pelvis of which six were bilateral). Precise fibrous dysplasia distribution was noted in 57 patients and we found that the femur was the more frequent localisation (47 have femur localisation cases and 10 had localisation only following pelvis localisation in 25 cases, six of them bilateral).Overall, of the 66 patients for whom data was available, 26 (39.39%) cases presented with a single myxoma and the remaining 40 cases presented multiple myxomas; 13 of them were bilateral, one was not specificated and 26 were unilateral (73.08% right and 26.92% left).In 60 patients, we knew the exact site; the most frequent localisation was the thigh (40 cases), followed by the pelvis with 17 cases.In 13 cases, the upper arm was involved and in six of these it was the sole site.

Signs and symptoms The following observations are based on 45 cases where clinical information was available.Myxomas can be painful or asymptomatic and noted only for increasing size. Myxoma can limit movement if located near a joint. Fibrous dysplasia was also asymptomatic nevertheless, in 10 cases, there was a history of pathological fractures most of them multiple. In 25 cases, there was associated McCune-Albright syndrome (five cases with only endocrine disturbances, 11 with “café au lait” spots and nine with both). The most frequent endocrine pathologies were thyroid problems and precocious puberty; one case of diabetes and three cases of Paget’s disease of the skull were also reported. Four cases of malignant change in FD are described in the literature, and it may be that malignant change is more common in Mazabraud’s syndrome [4, 5, 7, 11].

Conclusion

Although the association between fibrous dysplasia and myxomas is rare, it is probably underestimated because of frequent misdiagnosis. Females are twice as likely to be affected than males.

Fibrous dysplasia is usually diagnosed before or at the same time as the myxoma, following routine X-ray or magnetic resonance imaging.

Symptoms are related to the two different components; asymptomatic cases are common, so that pathological fractures and increasing size of painful or painless masses, may be present at the onset.

Endocrine disturbances, such as thyroid pathologies, growth disturbance and precocious sexual development, or “café au lait” spots can be associated in the McCune-Albright syndrome. The lower limbs are the most frequently affected. Fibrous dysplasia is more common in the femur and the pelvis, and myxomas in the quadriceps muscle. Nevertheless, all other sites are possible. When a myxoma is identified, careful examination may reveal further tumours since in over 70% they are multiple. In no case has there been continuity between tumours and bone lesions, although in most of them, there is a significant correlation between dysplastic bone and myxoma. Actually, although several hypotheses have been proposed, the aetiology of Mazabraud syndrome is still unclear.

The therapy for the myxoma is excision; fibrous dysplasia is only followed-up because there have been four cases of malignant change reported so that a high level of suspicion is mandatory.

Contributor Information

Carmine Zoccali, Phone: +39-338-6355040, Fax: +39-06-52662778, ti.orebil@ilaccozenimrac.

Giuseppe Teori, ti.ilacsit@iroet.

Umberto Prencipe, ti.ofi@epicnirp.

Fabio Erba, ti.ofi@abre.

References

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