Chițac, Celesta Drăgulescu, B. Petrescu, Alexandru Ciucă, M. Vasilca, A. We present the case of a year-old female patient, papilloma al naso oral haemorrhage and mild dysphagia. Clinical examination, flexible fibroscopy and imaging pointed to a diagnosis of a haemangioma of the right hypopharynx. A microscopic laryngoscopy procedure was carried out, with intratumoral monopolar electrocauterization which led to a complete retraction of the tumour.
The postoperative evolution was favourable, with no postoperative complications or recurrence up to 1-year check-up. Keywords haemangioma, angiography, monopolar electrocauterization Rezumat Autorii prezintă cazul unei paciente în vârstă de 31 de ani care se internează în clinica noastră pentru sângerare exteriorizată oral şi disfagie uşoară.
Pe baza examenului clinic, fibroscopic şi a investigaţiilor imagistice, se pune diagnosticul de formaţiune tumorală vasculară hipofaringiană dreaptă.
Se practică prin abord microlaringoscopic electrocauterizarea intratumorală cu ac monopolar, cu retracţia până la dispariţie a hemangiomului faringian. Evoluţia postoperatorie a fost bună, lipsită de complicaţii hemoragice sau dispnee. Nu s-a constatat recidivă tumorală la ultimul control efectuat la un an postoperator. Cuvinte cheie hemangiom angiografie cauterizare monopolară Case report Haemangiomas are benign tumours originating in the vascular endothelium.
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They represent a type of tumour rarely encountered in clinical practice, especially in the pharynx, papilloma al naso a small number of cases cited in literature. The treatment represents a challenge, as there is papilloma al naso agreed-upon standard, due to the rarity of the disease, the variable clinical aspect, and the location of the tumour.
A year-old woman consulted our clinic, accusing two episodes of oral haemorrhage, in moderate quantity, which ceased spontaneously, and mild dysphagia, all occurring in the last month. She had no record of other significant illness of herself or her family. She is a smoker and works as a clinical nurse. The physical examination and naso-pharyngeal-laryngeal fibroscopic examination revealed a polylobate sessile blueish tumour, approximately 1 cm in size, located in the right lateral hypopharyngeal wall, extending from the lower edge papilloma al naso the tonsil to the aryepiglottic fold Papilloma al naso 1.
No abnormalities were found in the larynx. Figure 1.
Semne şi simptome cancer de faringe Simptomele cancerului faringian includ: o formațiune dezvoltată la nivelul gâtului; modificarea vocii; dureri de cap și amețeli; tuse și dificultăți la înghițire; pierdere inexplicabilă în greutate; țiuit în urechi; leziuni la nivelul gurii care nu se vindecă. Aceste simptome pot fi, de asemenea, date de unele afecțiuni benigne, dar problemele persistente ar trebui evaluate de un medic. Simptomele cancerului faringian diferă în funcție de papilloma al naso lui, astfel: pentru cancerul orofaringian simptomele comune sunt dureri în gât persistente, dezvoltarea unei formațiuni la nivelul gurii sau gâtului, durere la nivelul urechii; în cazul cancerului hipofaringian, cele mai frecvente sunt problemele de înghițire și durerea la nivelul urechii; cancerul rinofaringian poate provoca papilloma al naso nazală, surditate și scurgeri nazale.
Papilloma al naso sessile tumour, blueish in color, with approximately 1 cm in size, situated on the right lateral hypopharinx wall Laboratory tests revealed no signs papilloma al naso anaemia or other pathological findings. After contrast administration, the lesion presented intense enhancement Figures 2 a, b and c.
Veruci vulgare 2. Veruci plantare 3. Veruci plane 4. Papiloame 5.
A digital subtraction angiography was carried out, with selective injection of internal, external carotid and vertebral arteries bilaterally and thyrocervical trunk, which did not reveal any tumoral enhancement or arterial feeders which could be embolised. Figure 2.
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Intravenous contrast axial CT showing intense fixation in the tumour; c. Intravenous contrast coronal CT Figure 3. A surgical approach under general anaesthesia was decided upon. Through microscope-aided direct laryngoscopy, electrocauterization is applied via a monopolar needle inserted into the tumour, until complete retraction of the tumour is achieved Figures 4 a, b and c.
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It is worth noting that no biopsy was carried out due to the very high risk of haemorrhage. The postoperative treatment consisted of intravenous antibiotic, non-steroid anti-inflammatory drugs and haemostatic drugs. Figure 4. Intraoperatory image, right hypopharingeal vascular tumour; papilloma al naso.
Electrocauterisation by a monopolar needle inserted into the tumour; c. Figure 5. Remission of the haemangioma and edema of the margin of the epiglottis and right arytenoid Next-day fibroscopic examination showed the complete remission of the vascular tumour and the presence of oedema of the right margin of the epiglottis and the right arytenoid, which diminished in the following papilloma al naso Figure 5.
The patient was discharged 9 days after the procedure. Further follow-ups at 1, 3, 6 and 12 months did not find any recurrence of the tumour Figure 6. Figure 6. Flexible fibroscopy image of the region on the day of discharge, showing no remaining tumour Discussion Haemangiomas are a class of benign tumours of vascular origin.
Hemangiomul faringian – caz clinic
They mostly develop in infants, with an incidence of 2. Despite this, they are rarely present at the moment of birth. They are found more often in people of Caucasian descent, with a ratio of females to males. They often have a phase of rapid progression followed by a period of stabilization and regression until the age of 7. Haemangiomas are found much less often in adult life and they have a different evolution, helmintox zales progressive growth and no spontaneous involution.
Less frequently, they can be found inside the oral cavity, more often on the lips or tongue, or in the nasal cavity, larynx or salivary glands. Pharyngeal localization is very rare, as there are a relatively small number of cases presented in literature.
The macroscopic aspect of a haemangioma is a globular tumour that is reddish or blue in colour, usually sessile, soft, incompressible, non-pulsating and papilloma al naso.
Much more than documents.
Sometimes it can be covered by normal mucosa, making it harder to differentiate. Its size varies from a few millimeters to several centimeters, with individual variation from supine to up-right position.
Histologically, they are classified into capillary and cavernous haemangiomas. They are characterized by endothelial proliferation and hyperplasia, increased turnover and in vitro capillary neoformation.
The Mulliken and Glowacki classification defines them as distinct from vascular malformations, with which they are often mistaken. The latter are present at birth and have a slow growth through endothelial turnover, with occasional rapid growth periods after local trauma, infections of hormonal changes.
Haemangiomas of the head and neck can be clinically silent papilloma al naso found during routine investigations or they may cause symptoms ranging from foreign body sensation hpv virus mann the oral cavity or throat, nasal obstruction, hearing impairment, dysphagia, dysphonia, up to severe dyspnoea, congestive heart failure or coagulopathy Papilloma al naso syndrome.
In some cases, epistaxis, oral haemorrhage or haemoptysis are the first symptoms to appear. Imaging procedures are crucial for the diagnosis of haemangiomas.
A papilloma al naso examination offers important information about the location and aspect papilloma al naso the tumour, but it cannot be used to estimate its extension.
A Doppler examination can indicate the vascular nature of the pathology. Intravenous contrast CT scan and MRI are important for determining the extension and nature of the haemangioma. MRI typically describes a lobulated, heterogeneous lesion, with well-defined ductal papilloma breast symptoms, with an intermediary signal papilloma al naso T1 and moderately-strong signal in T2, with intense signal enhancement after papilloma al naso administration of intravenous contrast agents.
Digital subtraction angiography can be particularly useful, as it can determine the presence of vascular pedicles, and may be used for embolization as a stand-alone treatment or before surgery. It is important papilloma al naso note that a biopsy may not be possible due to the high risk of bleeding. The differential diagnosis of haemangioma must take into account other vascular tumours, such as haemangiopericytoma, haemangioendothelioma, or angiofibroma. Other pathologies must be excluded: foreign body granuloma, submucosal hematoma, other benign tumours cysts, papilloma, fibroma, lymphangioma, lipoma, neurinoma, hamartoma, ectopic thyroid tissue or a malignant tumour most often, spinocelular carcinoma and sarcomas.
Hemangiomul faringian – caz clinic
The treatment of haemangiomas in ENT is difficult, as there is no agreed-upon standard. Most haemangiomas do not papilloma al naso treatment and are simply monitored. The pharmaceutical treatment is possible in juvenile cases where corticosteroids can be administered or, more recently, beta-receptor blockers.
Criocauterisation and sclerotherapy have been described with variable results.
Embolization may be attempted if papilloma al naso is a suitable vascular pedicle. Wherever possible, complete surgical excision is the most effective treatment method. Choosing any method must take into account the risks during and after surgery that derive from the vascular nature of the tumour. Possible complications include tissue necrosis, infection, oedema or hematoma of the surrounding regions, which can lead to acute respiratory distress, early and late post operatory bleeding, with possible flooding of the airways.
The patient must be properly informed regarding all these risks and must consent to the possibility of blood transfusion, vascular ligation or emergency tracheotomy, if necessary. The long-term evolution of haemangiomas is spontaneous involution in juvenile cases. In adults who have suffered surgery, recurrence is possible after 3 to 6 months.
The particular findings in the case presented: Very rare location of the tumour in an adult, at papilloma al naso pharyngeal level. Oral haemorrhage was the reason for consultation and discovery of the pathology. The diagnosis was based papilloma al naso imaging, instead of biopsy, due to the risk of bleeding close papilloma al naso the airways, which is difficult to control.
The surgical treatment is unstandardized and was decided upon after taking into account the risks during and bivalent human papillomavirus vaccine surgery due to the proximity of large vessels and the airways.
Este un vaccin care reduce drastic riscul de cancer de col uterin Cum stă treaba încă în țara noastră? Suntem pe primul loc în Europa la mortalitatea dată de acest tip de neoplasm.
Follow-up did not note any recurrence or complications up to the present date. Conclusion Haemangiomas are a class of benign vascular tumours, papilloma al naso in the ENT speciality, especially in adult life, which may remain hidden until severe symptoms appear, such as bleeding, dysphagia or dyspnoea. The diagnosis relies mainly in fibroscopic examination and imaging, while biopsy should be avoided due to the high risk of haemorrhage.
The lack of an international consensus on the treatment strategy represents a challenge for each patient individually. Choosing any method must take into account the natural progression of the disease, the papilloma al naso of treatment and the evolution after treatment. Conflict of interests: The authors declare no conflict of interests. Supraglotic hemangioma as papilloma al naso rare cause of recurrent hemoptysis: A new treatment modality with Argon plasma coagulation.
Facilitati de tratament
Lechien JR et al. Unusual presentation of an adult pedunculated hemangioma of the oropharinx. Clin Case Rep. Khil EK et al. Nasopharyngeal hemangioma in papilloma al naso A case report. J Korean Soc Radiol. Gangavati R et al. A review of hemangiomas of the oral cavity. Head and Neck Surgery, 16th edition.
BC Decker. Pyriform sinus haemangioma: an unusual presentation of an unusual condition.
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