12 results on '"PATOLOJİ"'
Number of results to display per page
Search Results
2. Collagenous Fibroma of the Caruncle: A Rare Pediatric Case.
- Author
-
BİLİCİ, Lara, MELİK, Ayşe Buse, BAHÇECİ ŞİMŞEK, İlke, and SAV, Aydın
- Subjects
FIBROMAS ,TUMORS in children ,HYPERPIGMENTATION ,HISTOPATHOLOGY ,COLLAGEN - Abstract
Copyright of Türkiye Klinikleri Journal of Ophthalmology is the property of Turkiye Klinikleri and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
- Published
- 2023
- Full Text
- View/download PDF
3. Oral Mukozal Lezyonlara Ait Histopatolojik Sonuçların Retrospektif Analizi.
- Author
-
ERSÖZ ÜNLÜ, Ceren, AKKOCA, Özlem, and ARSLAN, Necmi
- Abstract
The first evaluation according to the morphological features of the oral mucosal lesion gives us important information in terms of diagnosis and follow-up, however, the accurate diagnosis can be made after histopathological examination. In this study, the histopathological diagnoses of patients who underwent biopsy for oral mucosal lesions were evaluated. Material and Methods: The histopathological results of patients who underwent oral mucosal biopsies between 2009 and 2016 were evaluated according to the frequency of occurrence, localization, age and gender distribution of the diagnoses. Lesions were also grouped according to their characteristics of being benign non-neoplastic, benign neoplastic, premalignant, and malignant, and data were analyzed within groups. Results: Of the 340 patients, 193 (56.8%) were female and 147 (43.2%) were male. When the histopathological diagnoses were evaluated according to the groups, 177 (52.1%) patients had benign non-neoplastic, 126 (37.1%) patients had benign neoplastic, 14 (4.1%) patients had premalignant, and 23 (6.8%) patients had malignant lesions. Most of the malignant lesions were squamous cell carcinoma. The mean age of premalignant and malignant lesions was found to be significantly higher than the mean age of patients with benign lesions (p<0.001). Conclusion: Most of oral mucosal lesions are benign. Although the incidence of premalignant and malignant lesions increases with age, it should be kept in mind that they can also be seen in young patients. One of the most important points in the follow-up of oral mucosal lesions is the timely diagnosis and treatment of premalignant and malignant lesions. [ABSTRACT FROM AUTHOR]
- Published
- 2022
- Full Text
- View/download PDF
4. Mandibulada Görülen İntraosseöz Hemanjiyom: Nadir Bir Olgu Sunumu.
- Author
-
ERTÜRK, Ahmet Faruk, ATAPEK, Murat Mert, ÖZCAN, İlknur, and SOLUK TEKKEŞİN, Merva
- Subjects
TOOTH roots ,MAXILLOFACIAL surgery ,OPERATIVE dentistry ,RADIOPACITY ,COMPACT bone ,HYPODONTIA - Abstract
Copyright of Turkiye Klinikleri Journal of Dental Sciences is the property of Turkiye Klinikleri and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
- Published
- 2020
- Full Text
- View/download PDF
5. Chronic Cutaneous Lupus: A Case with Histopathological Mystery.
- Author
-
İNCEL UYSAL, Pınar, YALÇIN, Başak, BOZDOĞAN, Önder, and TAMER, Emine
- Subjects
- *
EDEMA , *LUPUS erythematosus , *ADIPOSE tissue diseases , *URTICARIA , *MUCINS , *PATIENTS - Abstract
Lupus erythematosus tumidus (LET) is a form of chronic cutaneous lupus which presents with erythematous urticaria like plaques on sun-exposed sites. Histologically, lack of epidermal alterations differentiates the LET from other cutaneous lupus variants. Perivascular and periadnexal lymphocytic infiltration and interstitial mucin deposition are the main microscopic characteristics. However, in the literature there are few reports that assert variation of the histopathological findings. From this point of view, we report here a male patient who is an interesting example of cutaneous lupus erythematosus with clinical behaviour of lupus tumidus but histological characteristics of discoid lupus. [ABSTRACT FROM AUTHOR]
- Published
- 2017
- Full Text
- View/download PDF
6. Sivas Numune Hastanesinde Baş-Boyun Bölgesine Lokalize Nonmelanositik Cilt Kanseri Şüphesiyle Plastik Cerrahi Kliniğine Konsülte Edilen Hastaların Değerlendirilmesi.
- Author
-
DEREBAŞINLIOĞLU, Handan, KURT ÖZKAYA, Neşe, and ALTINOK PARLAK, Burcu
- Abstract
Objective:We aimed to determine age, gender, localization area and types of lesions and reconstruction tecniques, suspicion of nonmelanoma skin cancer cases who were consulted from dermatology clinic localizated at head and neck. Material and Methods: Retrospective review of 163 patients undergoing exicion biopsy at the Sivas Numune Hospital Plastic Reconstructive Surgery Clinic for suspicion of nonmelanoma skin cancer localized at head and neck region, between January 2013 and December 2014 was undertaken. 176 excision material of 163 cases were searched. Results: In this study 163 patients (80; 49.07% males, 83; 50,9% females) were evaluated. Average of year was 60,4. Of the 175 exision material; 105 (60 %) were basal cell carcinoma, 13 (14.2%) were squamous cell carcinoma, 5 (2.8%) were basosquamous cell carcinoma, 25 (14.2%) were seboreic keratosis, 18 (10.2%) were keratoacanthoma, 6 (3.4%) were actinic keratosis, 1 (0.57%) was ruptured epidermal cyst rüptüre, 1 (0.57%) was inflammation, 1 (0.57%) granulation tissue. It was seen that the most common localization of nonmelanoma skin cancer was nose. Conclusion: In our study 176 of 124 (70.4%) exicion material were detected as nonmelanoma skin cancer, 176 of 24 (13.6%) exicion material were detected as premalign lesion. The most frequently seen nonmelanoma skin cancer was basal cell carcinoma followed by squamous cell carcinoma, malign basosquamous cell carcinoma. Therefore malign diagnose at nonmelanoma skin cancer was decided correctly 70,4% as clinically. [ABSTRACT FROM AUTHOR]
- Published
- 2016
- Full Text
- View/download PDF
7. Erişkin Tip Kolloid Milyum.
- Author
-
ŞAHİN, Aslı, VAHABOĞLU, Güler, ASTARCI, Hesna Müzeyyen, and EKŞİOĞLU, H. Meral
- Abstract
Colloid milium is a rare seen degenerative disease. Three different variant were described: adult, juvenile and nodular colloid degeneration. All of these variants have different ethiologic factors and also different clinical and histopatological appearances. Adult colloid milium has a dermal origin and chronic sun exposure is the most important ethiologic factor. Adult type is the most common above all variants. Mostly it effects middle aged and fair-skinned people. Males are effected four times more than females. Histopathologically, amorph eosinophilic materials expanding the papillary dermis and extending into the middle dermis. Solar elastosis is also present. Periodic Acid Schiff stains highlight the colloid material. Acral persistant pustular musinosis, nodular amyloidosis, syringoma, senile sebaceous hyperplasia must be thought as differential diagnoses. Histopathologically colloid milium is easily differentiated from all these. Though topical retinoids, dermaabrasion, diathermy, cryotherapy, Er-YAG laser are attempted for treating the disease, sun protection is the most recommended protective measure. In this report, unilaterally chronic sun exposed 53 years old taxi driver male with semilucent dome-shaped papules on his left ear helicis and left hand dorsum diagnosed clinically and histopathologically as colloid milium and treated with sunprotection agent and topical tretinoin was presented. The case was evaluated in the light of current literature. [ABSTRACT FROM AUTHOR]
- Published
- 2016
- Full Text
- View/download PDF
8. HHV-8-Related Three Malignancies in an Immunocompetent Patient: Kaposi Sarcoma, Multisentric Castleman Disease and Primary Effusion Lymphoma
- Author
-
Yusuf Ulusoy, Mahmut Töbü, Derya Demir, Mine Hekimgil, Hale Bülbül, Eren Arslan Davulcu, and Ege Üniversitesi
- Subjects
Pathology ,Mikrobiyoloji ,Tıbbi Laboratuar Teknolojisi ,Nörolojik Bilimler ,Radyoloji, Nükleer Tıp, Tıbbi Görüntüleme ,Transplantasyon ,Anatomi ve Morfoloji ,Sağlık Bilimleri ve Hizmetleri ,Enfeksiyon Hastalıkları ,Patoloji ,Dermatoloji ,Cerrahi ,Alerji ,Odyoloji ve Konuşma-Dil Patolojisi ,Hücre Biyolojisi ,Castleman disease ,virus diseases ,Tıbbi İnformatik ,Kadın Hastalıkları ve Doğum ,Onkoloji ,Periferik Damar Hastalıkları ,Psikiyatri ,Tropik Tıp ,Gastroenteroloji ve Hepatoloji ,Primary effusion lymphoma ,Sarcoma ,Romatoloji ,Biyoloji ,medicine.medical_specialty ,Temel Sağlık Hizmetleri ,Biyoteknoloji ve Uygulamalı Mikrobiyoloji ,Kalp ve Kalp Damar Sistemi ,Endokrinoloji ve Metabolizma ,Anestezi ,Biyofizik ,Klinik Nöroloji ,Üroloji ve Nefroloji ,Solunum Sistemi ,Acil Tıp ,Androloji ,medicine ,Spor Bilimleri ,Kulak, Burun, Boğaz ,Halk ve Çevre Sağlığı ,Geriatri ve Gerontoloji ,Genel ve Dahili Tıp ,Fizyoloji ,Göz Hastalıkları ,İmmünoloji ,business.industry ,Tıbbi Araştırmalar Deneysel ,medicine.disease ,Tıbbi Etik ,Adli Tıp ,Pediatri ,Ortopedi ,Hematoloji ,Tamamlayıcı ve Entegre Tıp ,Rehabilitasyon ,Biyokimya ve Moleküler Biyoloji ,Yoğun Bakım, Tıp ,business - Abstract
HHV-8 is associated with Kaposi sarcoma, multicentric Castleman disease and primary effusion lymphoma mostly in immunocompromised patients. in this report, we describe a female patient without any immunosuppressive state, encountering those three malignancies throughout her lifetime. A-69-year-old female patient was diagnosed with Kaposi sarcoma in 2009 and multicentric Castleman disease in 2011. She received several chemotherapy regimens during 4 years and stayed in remission during following 5 years. Then, she was diagnosed with primary effusion lymphoma, extracavitary/solitary variant on excisional biopsy of her cervical lymphadenopathy. Despite having 5 different lines of chemotherapy protocols, including autologous stem cell transplantation, and systemic cidofovir treatment, she died because of progressive disease. HHV-8 associated malignancies are not prevalent in immunocompetent patients. Our patient, who has suffered from all three malignancies related to HHV-8, is the only HIV negative patient in the literature with primary effusion lymphoma, extracavitary/solitary variant.
- Published
- 2019
9. Celiac Crisis: A Rare and Serious Condition Resulting in Death
- Author
-
Aydın Çifci, Özlem Gül Utku, İrfan Karahan, Gökberk Gözükan, and Kırıkkale Üniversitesi
- Subjects
Pediatrics ,Mikrobiyoloji ,Tıbbi Laboratuar Teknolojisi ,Nörolojik Bilimler ,Radyoloji, Nükleer Tıp, Tıbbi Görüntüleme ,Transplantasyon ,Medicine ,Anatomi ve Morfoloji ,Sağlık Bilimleri ve Hizmetleri ,Enfeksiyon Hastalıkları ,Patoloji ,Dermatoloji ,Cerrahi ,Alerji ,Odyoloji ve Konuşma-Dil Patolojisi ,Hücre Biyolojisi ,Tıbbi İnformatik ,Kadın Hastalıkları ve Doğum ,Onkoloji ,Periferik Damar Hastalıkları ,Psikiyatri ,Tropik Tıp ,Gastroenteroloji ve Hepatoloji ,Romatoloji ,Biyoloji ,medicine.medical_specialty ,Temel Sağlık Hizmetleri ,Biyoteknoloji ve Uygulamalı Mikrobiyoloji ,Kalp ve Kalp Damar Sistemi ,Endokrinoloji ve Metabolizma ,Celiac crisis ,Anestezi ,Biyofizik ,Klinik Nöroloji ,Üroloji ve Nefroloji ,Solunum Sistemi ,Acil Tıp ,Androloji ,Spor Bilimleri ,Kulak, Burun, Boğaz ,Halk ve Çevre Sağlığı ,Geriatri ve Gerontoloji ,Genel ve Dahili Tıp ,Fizyoloji ,Göz Hastalıkları ,İmmünoloji ,business.industry ,nutritional and metabolic diseases ,Tıbbi Araştırmalar Deneysel ,Tıbbi Etik ,digestive system diseases ,Adli Tıp ,Pediatri ,Ortopedi ,Hematoloji ,Tamamlayıcı ve Entegre Tıp ,Rehabilitasyon ,Biyokimya ve Moleküler Biyoloji ,Yoğun Bakım, Tıp ,business - Abstract
Celiac disease is an autoimmune disease of the small intestine, resulted from villusdamage and malabsorbtion due to ingestion of gluten; and production of antibodies to gliadin. Thedisease can manifest with various presentations. Celiac crisis was described as an acute, serious,life-threatening form of celiac disease about sixty years ago with a higher incidence among pediatric patients than adults. It is characterized by gastrointestinal symptoms like profuse diarrhea andsevere metabolic distubances like hyponatremia and hypoproteinemia. Early suspicion and detection is important. This case report presents a 54-year-old female patient who died from celiac crisis and sepsis.
- Published
- 2019
10. Recurrent Case of a Rare and Devastating Entity: Harlequin Ichthyosis
- Author
-
Özgür Kan, Aysegul Alkilic, Elif Nazlı Çetindağ Aydin, [Belirlenecek], TOBB ETU, Faculty of Medicine, Department of Surgical Sciences, TOBB ETÜ, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümü, and Alkılıç, Ayşegül
- Subjects
Mikrobiyoloji ,Tıbbi Laboratuar Teknolojisi ,Nörolojik Bilimler ,Radyoloji, Nükleer Tıp, Tıbbi Görüntüleme ,Transplantasyon ,Medicine ,Anatomi ve Morfoloji ,Sağlık Bilimleri ve Hizmetleri ,Enfeksiyon Hastalıkları ,Patoloji ,Dermatoloji ,Cerrahi ,Alerji ,Odyoloji ve Konuşma-Dil Patolojisi ,Hücre Biyolojisi ,Ichthyosis ,Tıbbi İnformatik ,Harlequin Ichthyosis ,Kadın Hastalıkları ve Doğum ,Onkoloji ,Periferik Damar Hastalıkları ,Psikiyatri ,Tropik Tıp ,Gastroenteroloji ve Hepatoloji ,Harlequin-type ichthyosis ,ichthyosis ,Romatoloji ,Biyoloji ,medicine.medical_specialty ,Temel Sağlık Hizmetleri ,Harlequin type ichthyosis ,Biyoteknoloji ve Uygulamalı Mikrobiyoloji ,Kalp ve Kalp Damar Sistemi ,Endokrinoloji ve Metabolizma ,Anestezi ,Biyofizik ,Klinik Nöroloji ,Üroloji ve Nefroloji ,Solunum Sistemi ,Acil Tıp ,Androloji ,Spor Bilimleri ,Kulak, Burun, Boğaz ,Halk ve Çevre Sağlığı ,Geriatri ve Gerontoloji ,Genel ve Dahili Tıp ,Fizyoloji ,Göz Hastalıkları ,İmmünoloji ,business.industry ,Tıbbi Araştırmalar Deneysel ,medicine.disease ,Tıbbi Etik ,Dermatology ,Adli Tıp ,Pediatri ,Ortopedi ,Hematoloji ,Tamamlayıcı ve Entegre Tıp ,Rehabilitasyon ,Biyokimya ve Moleküler Biyoloji ,Yoğun Bakım, Tıp ,business - Abstract
Harlequin ichthyosis (HI) is a rare and severe form of congenital ichthyosis caused by truncating mutations in the ABCA12 gene. Although it has many distinctive signs on perinatal sonography such as short limbs, wide gaping mouth, joint contractures, edema of the hands and feet and cloudy amniotic fluids, it usually can not be diagnosed until birth. Herein, we report a case of recurrent HI, which remained undiagnosed until labor at 38 weeks of gestational age. A multiparous woman presented to hospital at 38th weeks of gestation. There were no personal or family history. Vaginal delivery was performed and a 3300 gram baby was delivered. The body of the neonate was covered with thick, armor like skin, have generalized edema and erythematous fissures, scanty hair, everted eyelids with exposed swollen conjunctiva, open mouth were noted at the first examination. Newborn was diagnosed to be having Harlequin ichthyosis and was given to neonatal intensive care unit (NICU) for supportive care and additional examination. Genetic counseling is important and should be recommended to affected families. With the growing technology electron microscopes, invasive prenatal diagnostic tools and 3D sonography may reveal suggestive features of the disease. In addition, new treatment regimens, experienced and competent NICU facilities may increase survival rates.
- Published
- 2019
11. A Well Disguised Pleural Metastasis of Breast Carcinoma
- Author
-
Murat Sariçam
- Subjects
Pathology ,Mikrobiyoloji ,Pleural effusion ,Tıbbi Laboratuar Teknolojisi ,Nörolojik Bilimler ,Yoğun Bakım ,Transplantasyon ,Pleural metastasis ,Anatomi ve Morfoloji ,Sağlık Bilimleri ve Hizmetleri ,Enfeksiyon Hastalıkları ,Patoloji ,Dermatoloji ,Cerrahi ,Alerji ,Odyoloji ve Konuşma-Dil Patolojisi ,Hücre Biyolojisi ,Kulak ,Tıbbi İnformatik ,Kadın Hastalıkları ve Doğum ,Onkoloji ,Periferik Damar Hastalıkları ,Psikiyatri ,Tıp ,Tropik Tıp ,Gastroenteroloji ve Hepatoloji ,Romatoloji ,Breast carcinoma ,Biyoloji ,medicine.medical_specialty ,Temel Sağlık Hizmetleri ,Biyoteknoloji ve Uygulamalı Mikrobiyoloji ,Nükleer Tıp ,Kalp ve Kalp Damar Sistemi ,Burun ,Endokrinoloji ve Metabolizma ,Anestezi ,Biyofizik ,Radyoloji ,Klinik Nöroloji ,Tıbbi Görüntüleme ,Üroloji ve Nefroloji ,Solunum Sistemi ,Acil Tıp ,Androloji ,medicine ,Spor Bilimleri ,Halk ve Çevre Sağlığı ,Geriatri ve Gerontoloji ,Genel ve Dahili Tıp ,Fizyoloji ,Göz Hastalıkları ,İmmünoloji ,Boğaz ,business.industry ,Tıbbi Araştırmalar Deneysel ,medicine.disease ,Tıbbi Etik ,respiratory tract diseases ,Adli Tıp ,Pediatri ,Ortopedi ,Hematoloji ,Tamamlayıcı ve Entegre Tıp ,Rehabilitasyon ,Biyokimya ve Moleküler Biyoloji ,business - Abstract
Distant metastasis of breast carcinoma frequently occurs within five years after the diagnosis of the primary tumor. A 58-year-old female sharing a history of mastectomy for invasiveductal carcinoma six years previously admitted to our clinic with dyspnea progressively ongoing forpast two weeks. A right-sided massive pleural effusion was diagnosed and also pleural catheterdrained. Radiologic studies and cytological examination of the fluid did not introduce any evidenceof malignancy while she lately underwent thoracoscopy for the residuary effusion and atelectasis.Pathological study of the punch biopsies through the parietal pleura reported the pleural metastasis of the breast carcinoma but still negative evidence of malignancy for the pleural fluid. After discharge, evaluation with positron emission tomography also did not verify an uptake in any of thepleura, lungs or primary malignancy site. This event is of importance revealing that the patientssharing a past of malignancy should be approached with more caution and suspicion since the routine diagnostic algorithms pending to be reliable may not be applicable for all patients.
- Published
- 2019
12. Ileal Dieulafoy Lesion in a Patient with Glanzmann Thrombasthenia Presented with Hematochezia
- Author
-
Nilay Danis, Ömer Özütemiz, Abdullah Murat Buyruk, and Ege Üniversitesi
- Subjects
Mikrobiyoloji ,Tıbbi Laboratuar Teknolojisi ,Nörolojik Bilimler ,Gastroenterology ,Radyoloji, Nükleer Tıp, Tıbbi Görüntüleme ,Transplantasyon ,Thrombasthenia ,Medicine ,Anatomi ve Morfoloji ,Sağlık Bilimleri ve Hizmetleri ,Enfeksiyon Hastalıkları ,Patoloji ,Dermatoloji ,Cerrahi ,Alerji ,Odyoloji ve Konuşma-Dil Patolojisi ,Hücre Biyolojisi ,medicine.diagnostic_test ,Tıbbi İnformatik ,Kadın Hastalıkları ve Doğum ,Onkoloji ,Periferik Damar Hastalıkları ,Psikiyatri ,Glanzmann thrombasthenia ,Tropik Tıp ,Gastroenteroloji ve Hepatoloji ,medicine.symptom ,Romatoloji ,Biyoloji ,medicine.medical_specialty ,Temel Sağlık Hizmetleri ,Biyoteknoloji ve Uygulamalı Mikrobiyoloji ,Kalp ve Kalp Damar Sistemi ,Endokrinoloji ve Metabolizma ,Anestezi ,Biyofizik ,Klinik Nöroloji ,Lesion ,Üroloji ve Nefroloji ,Solunum Sistemi ,Acil Tıp ,Internal medicine ,Androloji ,Spor Bilimleri ,Kulak, Burun, Boğaz ,Halk ve Çevre Sağlığı ,Geriatri ve Gerontoloji ,Genel ve Dahili Tıp ,Fizyoloji ,Göz Hastalıkları ,İmmünoloji ,business.industry ,Tıbbi Araştırmalar Deneysel ,Tıbbi Etik ,Hematochezia ,Endoscopy ,Adli Tıp ,Pediatri ,Ortopedi ,Hematoloji ,Tamamlayıcı ve Entegre Tıp ,Rehabilitasyon ,Biyokimya ve Moleküler Biyoloji ,Yoğun Bakım, Tıp ,business - Abstract
Dieulafoy lesion (DL) is an important cause of acute gastrointestinal hemorrhage (GIH) because endoscopic diagnosis is very difficult. We report an ileal DL in a patient with Glanzmann Thrombasthenia (GT). A forty-year old female presented with bloody stool. Records showed that she was diagnosed with GT at 3 years of age. Physical examination on admission, she was clinically stable, except for tachycardia (110 bpm). Rectal examination revealed bright red blood. Her haemoglobin level was 8.7 g/dl. Colonoscopy revealed a DL at the terminal ileum. It was treated with combined endoscopic therapy of epinephrine injection followed by two clips application. Haemoglobin values were stable in the post-procedural period. DL in the terminal ileum is very rare. There have been fewer than 20 cases reported in the literature to date. Also GT is a rare congenital bleeding disorder. This case report revealed the coincidence of two rare disorders.
- Published
- 2019
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.