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Tytuł:
Sjögrens syndrom – the review of the latest diagnostic guidelines essential for otolaryngologists
Autorzy:
Kruk, Karolina
Rzepakowska, Anna
Osuch-Wójcikiewicz, Ewa
Niemczyk, Kazimierz
Powiązania:
https://bibliotekanauki.pl/articles/1399442.pdf
Data publikacji:
2019
Wydawca:
Index Copernicus International
Tematy:
autoimmune sialadenitis
dry mouth
dryness syndrome
sicca syndrome
Sjögren syndrome
Opis:
Sjogren’s syndrome (SS) is a complex connective tissue disease with autoimmune background and high clinical, radiological and molecular heterogeneity. SS is typically manifested by sicca syndrome, characterized by dry eyes and dry mouth due to autoimmune-induced inflammation of the lacrimal and salivary glands. Complications of sicca syndrome are dental caries, oral candidiasis, dysosmia, dysgeusia, difficulties in swallowing and chewing. SS may coexist with other diseases of rheumatoid and autoimmune etiology. SS is linked to an 16-fold increased risk of non-Hodgkin lymphoma. Early diagnosis results in appropriate treatment and may slow down the course of the disease and limit extraglandular involvement. Due to diverse clinical phenotypes and symptomatology, establishing of the diagnosis is often difficult. In 2016 the AmericanEuropean Consensus Group (AECG) and European League Against Rheumatism (EULAR) proposed a classification system that defines SS as a systemic disease. Diagnostic tools in establishing SS diagnosis are serological tests, ultrasonography, Schirmer’s test, unstimulated whole saliva flow rate and Ocular Staining Score. The complete curing of SS is still not possible. As a complex multisystem disease, SS requires multidisciplinary cooperation and individual diagnostic and therapeutic approaches in patients. Therapy is focused on the treatment of symptoms and prophylaxis of complications. The laryngological treatment of oral cavity symptoms in SS include supervision of proper oral hygiene habits and adequate fluids supplementation. The EULAR Sjögren’s syndrome disease activity index (ESSDAI) and Clinical Oral Dryness Score(CODS) are used to monitor disease progression and treatment effectiveness.
Źródło:
Polski Przegląd Otorynolaryngologiczny; 2019, 8, 2; 1-6
2084-5308
2300-7338
Pojawia się w:
Polski Przegląd Otorynolaryngologiczny
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Assessment of surgical treatment of Eagle’s syndrome
Autorzy:
Czajka, Marcin
Szuta, Mariusz
Zapała, Jan
Janecka, Iga
Powiązania:
https://bibliotekanauki.pl/articles/1397804.pdf
Data publikacji:
2019
Wydawca:
Index Copernicus International
Tematy:
Eagle’s syndrome
odynophagia
stylocarotid syndrome
styloid process
Opis:
Introduction: The aim of the study was to assess the effectiveness of surgical treatment of patients with Eagle’s syndrome, taking into account both early and late results. Material and methods: The study group consisted of 15 patients who underwent resection of the styloid process due to Eagle syndrome in the period of 2005–2017. During the follow-up visit, the patients were asked to fill in a post-operative questionnaire that compared the pre-operative symptoms and their severity with the patients’ current health condition. The VAS pain scale was used to assess each symptom, and the Laitinen scale was used to assess the quality of life. Data from patients’ medical records were also included. The results of the surveys were subjected to statistical analysis. Results: The study showed that in 11 out of 15 cases there was a significant improvement in the level of pain (70.5% on average) and an improvement in quality of life (on average 65%) comparing to the pre-operative condition. The Wilcoxon test for binding pairs, the Mann-Whitney test, the Kruskal-Wallis test and the Spearman correlation coefficient were used in the statistical analysis. There were statistically significant correlations between the recorded improvement rate and the length of the resected styloid process and its setting. Discussion: The study proved that resection of prolonged styloid process from extraoral approach in most cases is an effective method of treatment of Eagle syndrome, that carries low risk of complications.
Źródło:
Polish Journal of Otolaryngology; 2019, 73, 5; 18-24
0030-6657
2300-8423
Pojawia się w:
Polish Journal of Otolaryngology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Triple negative breast cancer with ACTH-dependent Cushings syndrome - case report
Autorzy:
Hodorowicz-Zaniewska, Diana
Brzuszkiewicz, Karolina
Szpor, Joanna
Powiązania:
https://bibliotekanauki.pl/articles/1392214.pdf
Data publikacji:
2019
Wydawca:
Index Copernicus International
Tematy:
breast cancer
paraneoplastic syndrome
ACTH
adrenocorticotropin
Cushing’s syndrome
Opis:
Introduction: Endocrine and metabolic paraneoplastic syndromes in the course of malignant tumors result from ectopic production of hormones or hormone precursors in tumor cells. Production of hormones by endocrine tumors is relatively frequent, while such production by adenocarcinoma cells is definitely rare. The study presents a case of triple-negative invasive breast cancer, with the ectopic secretion of ACTH (adrenocorticotropic hormone), which provokes serious metabolic disorders. Materials and methods: The patient was admitted to hospital with symptoms of Cushing`s syndrome. Diagnostic tests revealed that the cause of metabolic disorders was breast cancer. After proper preparation, the patient was qualified for surgery. Results: After the mastectomy, the patient’s metabolism stabilized. The patient underwent adjuvant chemotherapy and radiotherapy. Four months after the last cycle of systemic treatment, cancer dissemination was found. The patient was treated with second-line chemotherapy, however, control CT revealed progression. The patient died 20 months after surgery and two months after the last cycle of chemotherapy. Conclusions: The case reported in this study – triple-negative invasive breast cancer, responsible for ectopic production of ACTH and causing Cushing’s syndrome – is a rare phenomenon. Treatment of patients with breast cancer showing hormonal activity should not differ from general rules applied for breast cancer. However, due to accompanying metabolic disturbances, the patients need individualized oncological approach, precise diagnostic tests, and adequate preoperative preparation.
Źródło:
Polish Journal of Surgery; 2019, 91, 2; 45-47
0032-373X
2299-2847
Pojawia się w:
Polish Journal of Surgery
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Comparison of the incidence rates of coincident symptoms in a group of patients with Vertigo
Autorzy:
Šichnárek, Jakub
Vyskotová, Jana
Macháčková, Kateřina
Mrázková, Eva
Powiązania:
https://bibliotekanauki.pl/articles/1398471.pdf
Data publikacji:
2017
Wydawca:
Index Copernicus International
Tematy:
vertigo
vestibular disorders
central vestibular syndrome
peripheral vestibular syndrome
Opis:
ÚVOD: Závrať je druhým nejčastějším příznakem. kvůli kterému pacienti musí vyhledat lékaře. Efektivní léčba závrativých stavů vyžaduje spolupráci mnoha lékařských odvětní. CÍL: Cílem bylo analyzovat údaje z databáze pacientů s vertigem vyšetřených v Centru pro poruchy sluchu a rovnováhy v Ostravě – Porubě, zjistit, zda a v jakých faktorech se od sebe odlišují soubory pacientů s diagnostikovaným centrálním a periferním vestibulárním syndromem. METODIKA: výzkum byl proveden formou retrospektivní studie, která probíhala od října 2012 do února 2013. Data byla sbírána z dokumentace všech pacientů, kteří byli vyšetřeni otoneurologem na základě potíží s vertigem. VÝSLEDKY: Statisticky významný rozdíl byl nalezen mezi soubory s centrálním a periferním vertigem ve výskytu hypertenze, poruchy sluchu, zánětů středního ucha, mírné obezity a výsledky stabilometrického vyšetření. ZÁVĚR: Rozdíl mezi soubory s periferním a centrálním souborem jsou zmíněny výše. Mezi ostatními hledanými příznaky nebyl nalezen rozdíl. Výsledky potvrzují nutnost multioborového přístupu k pacientům s vertigem.
Źródło:
Polish Journal of Otolaryngology; 2017, 71, 1; 34-39
0030-6657
2300-8423
Pojawia się w:
Polish Journal of Otolaryngology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Porównanie częstości występowania objawów współistniejących w grupie pacjentów z zawrotami głowy
Autorzy:
Šichnárek, Jakub
Vyskotová, Jana
Macháčková, Kateřina
Mrázková, Eva
Powiązania:
https://bibliotekanauki.pl/articles/1398477.pdf
Data publikacji:
2017
Wydawca:
Index Copernicus International
Tematy:
vertigo
vestibular disorders
central vestibular syndrome
peripheral vestibular syndrome.
Opis:
BACKGROUND: Dizziness is the second most frequent symptom that make patients seek specialized examination. The effective solution of dizzy conditions requires treatment in cooperation with different branches of medicine. OBJECTIVE: To analyze data from the database of patients with vertigo examined in the Hearing and Balance Disorder Centre in Ostrava, to find out whether, and in what factors, the sets of patients with diagnosed central and peripheral vestibular syndrom differ from each other. METHODS: Retrospective study that was carried out from October 2012 to February 2013. The data was gathered from documentation of all vertiginous patients who were examined by an otoneurologist. RESULTS: The statistically significant difference between the two sets was found in: occurrence of hypertension and mild obesity, impaired hearing and otitis media, stabilometric testing CONCLUSIONS: There was a statistically significant difference between the sets with the central and peripheral vestibular syndrome in the frequency of occurrence of hypertension, impaired hearing, otitis media, in mild obesity categorization and in balance disorders. There was not any statistically significant difference found in the other observed factors. The results confirm the need of a multidisciplinary approach to patients with vertigo.
Źródło:
Polish Journal of Otolaryngology; 2017, 71, 1; 34-39
0030-6657
2300-8423
Pojawia się w:
Polish Journal of Otolaryngology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Gall-Stone Ileus – Own Patients And Literature Review
Autorzy:
Kozieł, Sławomir
Papaj, Piotr
Dobija-Kubica, Katarzyna
Śleziński, Przemysław
Wróbel, Józef
Powiązania:
https://bibliotekanauki.pl/articles/1395609.pdf
Data publikacji:
2015-05-01
Wydawca:
Index Copernicus International
Tematy:
gall-stone
gall-stone ileus
Bernard’s syndrome
Bouveret syndrome
cholelitchiasis
Opis:
Cholelithiasis is diagnosed in 10% of the population of the USA and Western Europe. A rare but serious complication of cholelithiasis is the obstruction of the digestive tract caused by a gall-stone (Bernard syndrome). It can add up to 1-4% of the mechanical obstructions of a small intestine among the general population but it can result in nonstriangulational mechanical obstructions of a small intestine in 25% cases among the patients over the age of 65. 5 patients have undergone an operation due to a small intestine gall-stone ileus in years 2011-2013 (within 27 months) in the General Surgery Ward of the Beskid Oncology Center - Municipal Hospital. In 4 patients simple enterotomy with a gall-stone extraction was performed. In the fifth patient enterolitotomy was conducted together with cholecystectomy and fistulotomy.
Źródło:
Polish Journal of Surgery; 2015, 87, 5; 260-267
0032-373X
2299-2847
Pojawia się w:
Polish Journal of Surgery
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Evaluation Of Irritable Bowel Syndrome Symptoms Amongst Warsaw University Students
Autorzy:
Niemyjska, Sylwia
Ukleja, Anna
Ławiński, Michał
Powiązania:
https://bibliotekanauki.pl/articles/1395637.pdf
Data publikacji:
2015-05-01
Wydawca:
Index Copernicus International
Tematy:
irritable bowel syndrome
IBS
Opis:
Irritable bowel syndrome (IBS) belongs to functional gastrointestinal disorders and is characterized by abdominal pain and change in stool consistency and/or bowel habits. Etiological factors include gastrointestinal peristalsis disturbances, visceral hypersensitivity, chronic inflammation of the mucous membrane, dysbacteremia, intestinal infections, psychosomatic and nutritional factors. Gastrointestinal motility disturbances in case of IBS are manifested by the inhibition of the intestinal passage, which favors the development of constipation or occurrence of diarrhea. The aim of the study was to evaluate IBS symptoms and demonstrate the relationship between physical activity and place of residence amongst Warsaw University students. Material and methods. The study was conducted in march, 2014 using a specific questionnaire, amongst Warsaw University students. The study group comprised 120 female patients, aged between 19 and 27 years (M=23.43; SD=1.29). The chi-square test was used for analysis, p<0.05 was considered as statistically significant. Results. The BMI of investigated patients ranged between 16.30-31.22 kg/m2 (M=21.27; SD=2.71). The majority of respondents (76.6%) weighed within the normal limits. Abdominal pain or discomfort occurred more frequently in the group of students who considered their physical activity as low. In case of respondents with a low physical activity bowel movement disorders and stool continence changes occurred more often, as compared to those with moderate physical activity. The most common symptom was rectal tenesmus, the least common-presence of mucous in the stool. Analysis showed that students with low physical activity were more frequently absent from school/work, due to abdominal symptoms. The respondents with moderate activity more often considered their abdominal symptoms, being associated with stress. Conclusions. IBS symptoms are common amongst Warsaw University students. In case of respondents with low physical activity, abdominal pain or discomfort occurred more often. It has been demonstrated that diet and stress might contribute to the occurrence of abdominal symptoms, being evidence of IBS.
Źródło:
Polish Journal of Surgery; 2015, 87, 5; 252-259
0032-373X
2299-2847
Pojawia się w:
Polish Journal of Surgery
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Chronic cough: new concepts and therapeutic possibilities
Autorzy:
Arcimowicz, Magdalenia
Niemczyk, Kazimierz
Powiązania:
https://bibliotekanauki.pl/articles/1401753.pdf
Data publikacji:
2016
Wydawca:
Index Copernicus International
Tematy:
cough
chronic cough
upper airway cough syndrome
Cough Hypersensitivity Syndrome
diagnosis
therapy
Opis:
Cough is the most common symptom of the upper and lower airway diseases. In its nature, cough is a defence re-flex mechanism of the respiratory tract that is used to clear the upper and lower airways. Chronic cough, defined as cough lasting for more than 8 weeks, is reported in 3–40% of the general population and has an important impact on patients’ quality of life, by causing anxiety, physical discomfort, social isolation and personal emabarrassment, be-ing an often medical complaint and one of the most common reasons for outpatient visits. Upper airway cough syn-drome, asthma, eosinophilic bronchitis and gastroesophageal reflux diseases account for most chronic cough after excluding somking, angiotensin-converting enzyme inhibitor use and chronic bronchitis. Many patients have more than one reason for chronic cough. Some complex diagnostic procedures, in many individuals are necessary to rec-ognized the cause/causes of chronic cough and to establish the accurate diagnosis, which implies a higher chance of effective treatment. Despite detailed diagnostic procedures, in many cases, the efficacy of chronic cough treatment is questionable and ambiguous. We observe not always satisfactory response to therapy. There are some coughs that seem refractory despite an extensive work-up. The possibility of hypersenitive cough reflex response, defining pa-tients with Cough Hypersensitivity Syndrome has been proposed to explain these cases, rather resistant to cough treatment, previously known as idioapthic cough or refractory, unexplained cough. The concept of Cough Hypersen-sitivity Syndrome helps us to understand the mechanisms underlying cough and provides better therapeutic options to treat chronic cough, like neuromodulating drugs, and speech therapy.
Źródło:
Polski Przegląd Otorynolaryngologiczny; 2016, 5, 1; 22-29
2084-5308
2300-7338
Pojawia się w:
Polski Przegląd Otorynolaryngologiczny
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Boerhaave Syndrome – over 290 years of surgical experiences. Can the disorder recur?
Autorzy:
Rokicki, Marek
Rokicki, Wojciech
Moj, Małgorzata
Bsoul, Tamer
Rydel, Mateusz
Powiązania:
https://bibliotekanauki.pl/articles/1391953.pdf
Data publikacji:
2019
Wydawca:
Index Copernicus International
Tematy:
esophageal perforation
Boerhaave syndrome
recurrence
Opis:
Spontaneous perforation of the esophagus (Boerhaave syndrome) is a rare disease that poses a serious surgical challenge. The analysis of literature concerning the Boerhaave syndrome reveled cases of recurrent spontaneous perforation of the esophagus. The incidental nature of this condition calls for more accurate assessment of all such cases. The authors made a detailed evaluation of the data obtained from eight reports of recurrent Boerhaave syndrome. The data is presented as a summary table comparing the clinical course and outcomes of patients with the primary Boerhaave syndrome as well as recurrent Boerhaave syndrome.
Źródło:
Polish Journal of Surgery; 2019, 91, 3; 27-29
0032-373X
2299-2847
Pojawia się w:
Polish Journal of Surgery
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Critical Upper Limb Ischemia Caused by Initially Undiagnosed Thoracic Outlet Syndrome - Case Report
Autorzy:
Dzieciuchowicz, Łukasz
Włodarczyk, Wojciech
Oszkinis, Grzegorz
Powiązania:
https://bibliotekanauki.pl/articles/1396624.pdf
Data publikacji:
2012-02-01
Wydawca:
Index Copernicus International
Tematy:
limb ischemia
thoracic outlet syndrome
Opis:
A case of a progressive ischemia of the right upper extremity in a 57-year-old male caused by primarily undiagnosed compression of a subclavian artery by an accessory cervical rib is presented. Critical limb ischemia persisting for 7 years despite conservative treatment and a thrombectomy of upper extremity arteries and thoracic sympathectomy, led to a loss of three fingers and development of a non-healing ulceration of right upper extremity. Eventually a cervical rib resection together with a subclavio-brachial venous bypass graft permanently reversed the critical limb ischemia and allowed the ulceration to heal.The presented case underscores the importance of an early surgical intervention in patients with upper limb ischemia and anatomic abnormalities in a thoracic outlet.
Źródło:
Polish Journal of Surgery; 2012, 84, 3; 158-162
0032-373X
2299-2847
Pojawia się w:
Polish Journal of Surgery
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Barogenic rupture of esophagus (Boerhaave syndrome) as diagnostic and therapeutic challenge requiring rapid and effective interdisciplinary cooperation – case report
Autorzy:
Czopnik, Piotr
Aporowicz, Michał
Niepokój-Czopnik, Agnieszka
Szajerka, Tobiasz
Domosławski, Paweł
Powiązania:
https://bibliotekanauki.pl/articles/1393124.pdf
Data publikacji:
2017
Wydawca:
Index Copernicus International
Tematy:
Boerhaave’s syndrome
mediastinitis
oesophageal fistula
Opis:
We describe a 47-year-old male who was admitted to our centre from a local emergency unit with septic shock due to suspected Boerhaave syndrome. After the diagnosis was confirmed, the patient underwent emergency surgery. Postoperatively, the patient had symptoms of acute alcoholic delirium, and developed an oesophagomediastinal fistula as the most serious local complication. Successful conservative treatment enabled complete healing of the fistula, leading to patient recovery. No late complications like oesophageal stenosis were found at 6 months from discharge.
Źródło:
Polish Journal of Surgery; 2017, 89, 6; 37-39
0032-373X
2299-2847
Pojawia się w:
Polish Journal of Surgery
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Own experience in the diagnosis and treatment of elongated styloid process syndrome
Autorzy:
Wacławek, Magdalena
Pietkiewicz, Piotr
Niewiadomski, Piotr
Olszewski, Jurek
Powiązania:
https://bibliotekanauki.pl/articles/1397274.pdf
Data publikacji:
2021
Wydawca:
Index Copernicus International
Tematy:
diagnostics
elongated styloid process syndrome
treatment
Opis:
Introduction: The aim of the study was to present selected cases with Eagle’s syndrome diagnosed and treated at the Department of Otolaryngology, Laryngological Oncology, Audiology and Phoniatrics, Medical University of Lodz, in the years 2016–2020. Material and method: Five selected clinical cases with Eagle’s syndrome are presented, including three male patients and two female patients, aged 28 to 42 years. Results: The prevalence of Eagle’s syndrome was similar for both female and male patients. The carotid artery syndrome, which is characterized by: visual disturbances, unilateral pain located along cervical vessels, headache and migraine, was more common. Lack of proper diagnosis of Eagle’s syndrome often significantly delays the implementation of proper treatment and thus exposes patients to long-term struggle with pain. Our observations have shown that the time between the onset of symptoms and correct diagnosis in patients averaged about five years. 3D-CT scan is the gold standard for detecting Eagle’s syndrome. An intraoral approach was used in surgical treatment. Although this approach offers shorter treatment time and better cosmetic effect, there is also a greater risk of complications associated with limited visibility of the surgical field and infection. Conclusions: Although styloid syndrome usually occurs bilaterally, these patients reported unilateral symptoms. No correlations were found between the prevalence of Eagle’s syndrome and sex, the length of the styloid process or age, nor side of the body. The best healing effect is obtained by surgical correction/reduction of the elongated styloid process.
Źródło:
Polish Journal of Otolaryngology; 2021, 75, 2; 21-27
0030-6657
2300-8423
Pojawia się w:
Polish Journal of Otolaryngology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Horners syndrome during spindle cell lipoma of theneck–a case report
Autorzy:
Kaczmarczyk, Dariusz
Kubiak, Marcin
Komoń-Kotecka, Ewa
Bartoszewicz, Robert
Bruzgielewicz, Antoni
Powiązania:
https://bibliotekanauki.pl/articles/1401930.pdf
Data publikacji:
2014
Wydawca:
Index Copernicus International
Tematy:
Spindle cell lipoma
Immunohistochemistry
Horner's syndrome
Opis:
Horner's syndrome is most often caused by a tumour compressing the sympathetictrunk. Spindle cell lipoma (SCL) is a rare tumour, corresponding to just 1.5% of the benigntumours of soft tissues. Its most common localisation is subcutaneous tissue in theupper part of the body. This paper presents a rare case of Horner's syndrome caused bya SCL of the neck.A 42-year-old male patient was admitted to the ENT Ward of the Mazovian SpecialHospital in Siedlce because of a neck tumour on the left side. Laryngological examinationrevealed only a hard tumour with a limited mobility on the left side of the neck. Oph-thalmological and neurological consultations indicated Horner's syndrome. Fine-needleaspiration biopsy gave no clear diagnosis. The patient was qualified for surgery. Thetumour was radically excised and sent for histopathological examination. Thefinal his-topathological diagnosis was: SCL. Symptoms of the Horner's syndrome disappearedwithin 3 weeks after the surgery.The discussed case should be noted because of untypical SCL localisation within thecervical perivascular space, and also because of presence of symptoms of Horner's synd-rome caused by compression of the tumour on the sympathetic trunk that disappearedfollowing the surgical treatment.
Źródło:
Polski Przegląd Otorynolaryngologiczny; 2014, 3, 4; 222-225
2084-5308
2300-7338
Pojawia się w:
Polski Przegląd Otorynolaryngologiczny
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Stridor as one of the symptoms of 5p deletion syndrome in a five-month-old child
Autorzy:
Malicka, Katarzyna
Grochowska-Bohatyrewicz, Ewa
Pietrzyk, Aleksandra
Iwona, Stecewicz
Jaworowska, Ewa
Giżewska, Maria
Powiązania:
https://bibliotekanauki.pl/articles/1400400.pdf
Data publikacji:
2017
Wydawca:
Index Copernicus International
Tematy:
5p deletion syndrome
5p minus syndrom
Cri du Chat syndrome
stridor
larynx malformations
laryngeal cleft
Opis:
The 5p deletion syndrome (5p-, Cri-du-chat syndrome, CdCS) is a genetic disorder which results from a partial deletion of the short arm of chromosome 5. It was first described by Lejeune et al. in 1963. The incidence ranges from 1:15 000 to 1:50 000 live births. The 5p- is usually diagnosed in the first days of life because of the characteristic monotonous high pitched cat-like cry and relatively constant dysmorphic features. Other symptoms often present in the neonatal period include low birth weight, muscle hypotonia, asphyxia and feeding difficulties due to impaired suction and swallowing, which may all lead to failure to thrive. Organ malformations, with various larynx abnormalities, although not very frequent, can also be present. Symptoms that are prevalent in later life include severe motor delay and intellectual disability with significant speech impairment, as well as behavioral problems. The case report presents a female infant in her 5th month of life in whom, despite the typical symptoms of 5p-, stridor and episodes of choking were the main problems. Laryngotracheal endoscopy revealed the type I laryngeal cleft. Genetic analysis confirmed the diagnose of 5p- syndrome. The presented case shows that it is critically important to perform a further investigation and refer a child with laryngological problems coexisting with dysmorphic features to a clinical geneticist.
Źródło:
Polski Przegląd Otorynolaryngologiczny; 2017, 6, 3; 41-46
2084-5308
2300-7338
Pojawia się w:
Polski Przegląd Otorynolaryngologiczny
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Skin and mucosal lesions in otolaryngological practice
Autorzy:
Sobolewski, Piotr
Ziuzia, Laura
Dobrzyński, Paweł
Walecka, Irena
Powiązania:
https://bibliotekanauki.pl/articles/1400416.pdf
Data publikacji:
2017
Wydawca:
Index Copernicus International
Tematy:
otolaryngology
dermatology
skin lesions
mucosal lesions
pemphigus
pemphigoid
Behçet's disease
lichen planus
Stevens - Johnson syndrome
Lyell's syndrome
Opis:
Cutaneous and mucosal lesions are seen in many diseases, frequently being the main element of the clinical presentation. It is not uncommon that the patient with mucosal lesions of the upper respiratory tract consults the otolaryngologist first, therefore it is important that those specialists know the mucosal symptoms of dermatological diseases and consider them in the differential diagnosis. In this article diseases with the mucosal lesions of the upper respiratory tract are described, including pemphigus, pemphigoid, lichen planus, and Behçet’s disease. Knowledge of the morphology of these mucosal manifestations is essential in the clinical practice of both dermatologists and otolaryngologists, and the diagnostic and therapeutic success may be achieved only with the cooperation of these specialists.
Źródło:
Polski Przegląd Otorynolaryngologiczny; 2017, 6, 3; 34-40
2084-5308
2300-7338
Pojawia się w:
Polski Przegląd Otorynolaryngologiczny
Dostawca treści:
Biblioteka Nauki
Artykuł
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