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B Coupe

Publications and source records attributed to B Coupe.

4 recordsLinked to original sources

Familial hypercholesterolaemia commonly presents with Achilles tenosynovitis.

BACKGROUND: Patients with heterozygous familial hypercholesterolaemia (HeFH) develop tendon xanthomata (TX), most commonly in their Achilles tendons. Even before tendons are chronically enlarged, tenosynovitis may occur and medical advice be sought. Untreated HeFH carries a high risk of premature coronary heart disease, which can be ameliorated by early diagnosis. OBJECTIVE: To determine the prevalence of episodes of Achilles tendon pain in HeFH before its diagnosis. METHODS: Patients with definite HeFH (Simon Broome criteria) attending a lipid clinic were identified. They completed a questionnaire asking about symptoms relating to their Achilles tendons. Unaffected spouses or cohabiting partners served as controls. RESULTS: 133 patients (47% men) and 87 controls (51% men) participated. TX had been recognised by the referring physicians in <5% of cases. However, 62 (46.6% (95% confidence interval (CI) 38.1 to 55.1)) patients had experienced one or more episodes of pain in one or both Achilles tendons lasting >3 days, whereas only 6 (6.9% (1.6 to 12.2)) controls had done so (difference p<0.001; likelihood ratio 6.75). Typically, in the patients with HeFH the pain lasted 4 days (median). It was described as severe or very severe in 24/62 (38.7% (30.4 to 47.0)) patients with HeFH, but never more than moderate in controls. 35 (26.3% (18.8 to 33.8)) patients with HeFH had consulted a doctor about Achilles tendon pain, but in no case had this led to a diagnosis of HeFH. None of the controls had consulted a doctor. CONCLUSIONS: Measurement of serum cholesterol in patients presenting with painful Achilles tendon could lead to early diagnosis of HeFH.

Achilles Tendon↗

[Myasthenia and Basedow's hyperthyroidism].

The authors report an exceptional case of myasthenia gravis associated with Graves' disease. Myasthenia gravis appeared at age 8 years. Hyperthyroidism was diagnosed at age 12 1/2 and quickly worsened, with signs of cardiothyrotoxicosis. In addition to the diagnostic difficulties, the immunologic origin seems to be implicated in these diseases. Thymectomy associated with subtotal thyroidectomy was performed, with good results during an 18 months follow-up.

Child↗

[Bilateral hamartoma of the chest wall].

Because its extreme rarity, a case of a bilateral chest wall hamartoma is reported in an 7 months infant presenting a moderate thoracic deformation. Roentgenogram reveals a segmentary costal destruction and an adjacent intrathoracic mass. A right thoracotomy is realized and the tumor is removed without difficulties. Diagnosis of a vasculo-cartilaginous hamartoma (other term used: mesenchymoma) is confirmed after the resection of the right lesion, whereas the left one is spontaneously reducing within 7 months. After analysis of 20 previously reported identical cases, we think that diagnosis may be done on clinico-radiological grounds; surgical decision has to take into account the constant benignity, the possible spontaneous regression and the orthopedic sequelae due to an extensive resection.

Female↗