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            [0] => Nora lesion: Diagnosis, Treatment and Clinical Follow-up. Case report.
        )

    [etablissement] => Array
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            [0] => hôpital FSI la Marsa
        )

    [nom] => Array
        (
            [0] => BEN ROMDHANE
        )

    [prenom] => Array
        (
            [0] => Majdi
        )

    [email] => Array
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            [0] => majdi.benromdhane@fmt.utm.tn
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            [0] => 22635981
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            [0] => 
 
Nom prénom / Name Surname: Zaafouri Akram
Email: zaafouri1994@gmail.com
Hôpital / Hospital: hôpital FSI la Marsa

 
Nom prénom / Name Surname: Ben Romdhane Majdi
Email: majdi.benromdhane@fmt.utm.tn
Hôpital / Hospital: hôpital FSI la Marsa

 
Nom prénom / Name Surname: Kamoun Haithem
Email: haithem.kamoun@fmt.utm.tn
Hôpital / Hospital: hôpital FSI la Marsa

 
Nom prénom / Name Surname: Sghaier Majdi
Email: sgh.majdi@gmail.com
Hôpital / Hospital: hôpital FSI la Marsa

 
Nom prénom / Name Surname: Elafram rafik
Email: rafik.elafram@gmail.com
Hôpital / Hospital: hôpital FSI la Marsa

        )

    [mots_cles] => Array
        (
            [0] => nora lesion, tumor, osteochondromatous;

        )

    [event-id] => Array
        (
            [0] => 3663
        )

    [statut] => Array
        (
            [0] => 1
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            [0] => none
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    [user_email] => Array
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            [0] => majdi.benromdhane@fmt.utm.tn
        )

    [specialite] => Array
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            [0] => Chirurgie orthopédique et traumatologique
        )

    [pays] => Array
        (
            [0] => Tunisie
        )

    [texte_abs] => Array
        (
            [0] => Introduction : 
NORA tumor, or bizarre parosteal osteochondromatous proliferation, is a rare entity affecting the long bones of the hands and feet of patients in their fourth decade. The positive diagnosis is suspected on the basis of non-specific radiological signs, and is confirmed by anatomopathological examination. Although generally benign, these tumors can lead to significant functional complications, and a very high risk of recurrence, which justifies increased attention to their evaluation, treatment and follow-up.
Methods: 
We report the case of a 38-year-old patient with no notable pathological history who presented a NORA tumor in the second phalanx of the 3rd finger treated surgically.
Results: 
In this case study, we examined a patient with Nora's tumor, which is a rare and complex condition. The clinical examination and radiological findings were non-specific. Intraoperatively, the macroscopic appearance of the lesion suggested a NORA tumor, which was confirmed histologically. At one year's follow-up, the patient showed no functional discomfort and no clinical or radiological signs of recurrence.
Discussion : 
The diagnostic approach and treatment adopted in our case is similar to that described in the literature, despite the fact that reported cases of this pathology remain sporadic.
Conclusion : 
NORA tumor is a rare entity whose diagnosis is suspected on the basis of a number of clinical and radiological findings, but is only confirmed histologically. Treatment is complete surgical resection, to reduce the risk of recurrence, which remains the most frequent complication.
Diagnostic analysis, therapeutic approaches and clinical follow-up illustrate the challenges encountered in managing this rare pathology.
        )

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