[Thyroglossal duct cyst carcinoma: The rational behind performing a total thyroidectomy]. / Prise en charge du carcinome papillaire du kyste du tractus thyréoglosse: Intérêt de la thyroïdectomie totale.

Thyroglossal duct cysts are a common developmental abnormality but carcinoma within is rare. A 68 year old male patient was diagnosed with a thyroglossal duct cyst (TGDC) which on imaging studies demonstrated suspicious features within the cyst alone. Fine needle aspiration cytology was suspicious of papillary thyroid cancer. A Sistrunk's procedure (SP) was performed and demonstrated papillary carcinoma within. A decision to perform a total thyroidectomy (TT) and central compartment neck dissection was made. Final histological analysis showed no disease within the thyroid gland or in the neck nodes. The presence of cancer suspected within the TGDC by relevant diagnostic modalities may necessitate treatment to the thyroid gland and neck in addition to a Sistrunk's procedure as part of a definitive treatment policy due to the high incidence of associated thyroid malignancy. In our institution, in patients presenting with thyroglossal duct cyst carcinoma and are at high risk for having thyroid cancer, we perform both SP as well as TT and central compartment neck dissection.

Les kystes du tractus thyréoglosse (KTT) sont fréquents et leur dégénérescence est rare. Nous rapportons le cas d'un patient de 68 ans avec un diagnostic de KTT et une imagerie démontrant des caractéristiques suspectes au sein du kyste. La ponction cytologique réalisée était suspecte de carcinome papillaire sur KTT. La procédure de Sistrunk (PS) a été réalisée et a confirmé la présence du cancer papillaire au sein du kyste. La décision de réaliser une thyroïdectomie totale (TT) associée à un curage du compartiment central cervical a été retenue. L'examen histologique a montré l'absence de lésions suspectes dans la glande thyroïde ainsi qu'au niveau des ganglions cervicaux. La suspicion de cancer au sein du KTT révélée par des modalités de diagnostic pertinentes peut nécessiter un traitement chirurgical de la glande thyroïde ainsi que des ganglions cervicaux, en plus de la procédure de Sistrunk, dans le cadre d'une politique de traitement définitif en raison de la forte incidence de malignité au sein de la glande thyroïde. Dans notre institution, chez les patients présentant un carcinome du KTT qui sont à risque élevé d'avoir un cancer de la thyroïde associé, nous réalisons la PS, une thyroïdectomie totale ainsi qu'un curage du compartiment central cervical.

[Techniques and strategy of pathological sampling in the diagnostic and therapeutic management of lung cancer]. / Techniques et stratégie de prise en charge des prélèvements anatomopathologiques dans le cadre de l'approche diagnostique et thérapeutique du cancer bronchique.

Histopathology is key to the diagnosis and staging of lung cancer. This analysis requires tissue sampling from primary and/or metastatic lesions. The choice of sampling technique is intended to optimize diagnostic yield while avoiding unnecessarily invasive procedures. Recent developments in targeted therapy require increasingly precise histological and molecular characterization of the tumor. Therefore, pathologists must be economical with tissue samples to ensure that they have the opportunity to perform all the analyses required. More than ever, good communication between clinician, endoscopist or surgeon, and pathologist is essential. This is necessary to ensure that all participants in the process of lung cancer diagnosis collaborate to ensure that the appropriate number and type of biopsies are performed with the appropriate tissue sampling treatment. This will allow performance of all the necessary analyses leading to a more precise characterization of the tumor, and thus the optimal treatment for patients with lung cancer.

[Pulmonary granulomatous necrotizing vasculitis: an extra-intestinal manifestation of ulcerative colitis or Wegener's granulomatosis?]. / Vasculite granulomateuse nécrosante pulmonaire : une manifestation extra-intestinale de la rectocolite ulcéro-hémorragique ou une maladie de Wegener isolé ?

Respiratory symptoms are rare manifestations of ulcerative colitis as well as intestinal manifestations in Wegener granulomatosis. We report the case of a 17-year old man previously diagnosed as having ulcerative colitis who presented with diffuse thoracic pain. Hypermetabolic pulmonary nodules were discovered at the positron emission tomographic scan. Necrotizing granulomatous vasculitis was demonstrated at lung biopsy. In this paper, we describe the association between pulmonary nodules and ulcerative colitis and we discuss the possibility of an overlap syndrome between ulcerative colitis and Wegener granulomatosis.

Localized malignant lymphohistiocytoid pleural mesothelioma.

We report a case of a 42-year-old man with a right pleural mesothelioma. This neoplasm has 3 rare features. Firstly, it was a localized form: suspected by imaging, visualized by video-assisted thoracoscopy, at the time of the curative-thoracotomy and confirmed by the pathological analysis. The second characteristic is its histological type: "malignant lymphohistiocytoid mesothelioma". This rare subtype has been reported in only 4 papers. Third, after pleuro-pneumonectomy, our patient is alive after 6 years and 5 months postoperatively without any sign of recurrence. Only one case with a long follow-up has been reported but with recurrence at 5 years postoperatively.

The management of a pulmonary artery aneurysm.

A 51-year-old woman with a giant pulmonary artery aneurysm was referred to our department for surgical opinion. Imaging study confirmed a large aneurysmal dilatation of the left pulmonary artery starting in the pulmonary trunk. There was no underlying pathology except for a pulmonary commissurotomy 20 years previously for a significant valvular pulmonary stenosis. The role of surgery in this entity is not well defined. We report the management of one case.

Consensus: the follow-up of the treated patient.

This is the first consensus document on the follow-up of the treated patient with non-small cell lung cancer that has been written by this group. The document has been drawn up by doctors coming from many different cultures and philosophical backgrounds. It acknowledges that there are published guidelines on the follow-up particularly those in trials, and does not wish to contradict these. There is lack of evidence-based medicine to recommend a strong general policy in this area. For those patients who were treated with curative intent the initial follow-up will depend upon the toxicity that is evident from the treatment given. Thereafter the interval between follow-up visits should be every 3 months for the first two years, then every 6 months for up to five years. Rapid and easy access to the multidisciplinary team should be available. Full examination and chest X-ray should be carried out on each visit but other investigations should be determined by clinical need. For those patients treated with palliative intent the interval between follow-up visits once the acute reactions have settled will depend upon the adequacy of the control of the symptom and the availability of separate palliative care teams. At all times the patient should have rapid access to the multidisciplinary team and in general frequent follow-up, that is at intervals of one to two months, may be appropriate during the first six months. Follow-up constitutes an important part of lung cancer management. Efforts should be made to gain clinical material to give us evidence-based guidelines.

Intrinsic positive end-expiratory pressure during one-lung ventilation of patients with pulmonary hyperinflation. Influence of low respiratory rate with unchanged minute volume.

BACKGROUND: We measured lung mechanics and gas exchange during one-lung ventilation (OLV) of patients with chronic obstructive pulmonary disease, using three respiratory rates (RR) and unchanged minute volume. METHODS: We studied 15 patients about to undergo lung surgery, during anaesthesia, and placed in the lateral position. Ventilation was with constant minute volume, inspiratory flow and FIO2. For periods of 15 min, RR of 5, 10, and 15 bpm were applied in a random sequence and recordings were made of lung mechanics and an arterial blood gas sample was taken. Data were analysed with the repeated measures ANOVA and paired t-test with Bonferroni correction. RESULTS: PaO2 changes were not significant. At the lowest RR, PaCO2 decreased (from 42 (SD 4) mm Hg at RR 15-41 (4) mm Hg at RR 10 and 39 (4) mm Hg at RR 5, P<0.01), and end-tidal carbon dioxide increased (from 33 (5) mm Hg at RR 15 to 35 (5) mm Hg at RR 10 and 36 (6) mm Hg at RR 5, P<0.01). Intrinsic positive end-expiratory pressure (PEEPi) was reduced even with larger tidal volumes (from 6 (4) cm H2O at RR 15-5 (4) cm H2O at RR 10, and 3 (3) cm H2O at RR 5, P<0.01), most probably caused by increased expiratory time at the lowest RR. CONCLUSION: A reduction in RR reduces PEEPi and hypercapnia during OLV in anaesthetized patients with chronic obstructive lung disease.

[Cap polyposis: a rare syndrome]. / Cap polyposis: un syndrome rare.

We report a case of inflammatory cap polyposis of the colon, a rare syndrome, affecting the rectosigmoid. It was observed in a context of mucous diarrhea. Endoscopic and radiological features consisted of elevated and umbilicated nodular lesions. Histology revealed polypoid lesions containing elongated crypts with superficial abrasions, covered by inflammatory and fibrinoid material. Etiopathogenesis of this new syndrome is unknown.

Camurati-Engelmann disease. Effects of corticosteroids.

Camurati-Engelmann disease is an uncommon condition, radiologically characterized by symmetric diaphyseal sclerosis involving the tubular bones. Clinical features include limb pain, muscle weakness, waddling gait and sometimes deafness. The evaluation is made by conjunction of radiographic and scintigraphic data. Corticosteroids and analgesics improve the quality of life, decrease the pain but do not alter the course of the disease. The evolution is unpredictable. The history of a 23 year old male with such a disorder is presented hereafter. His clinical course shows a very good response to the administration of corticosteroids, whereas no improvement is observed as far as the radiographic and isotopic features are concerned.