scholarly journals Clinical and endoscopic diagnosis of MALT-lymphoma of the duodenum

2021 ◽  
Vol 1 (5) ◽  
pp. 82-85
Author(s):  
I. Yu. Korzheva ◽  
N. E. Chernekhovskaya ◽  
A. A. Razzhivina ◽  
N. A. Hayrapetyan ◽  
A. E. Tyurin
Keyword(s):  
Rare Disease ◽  
Malt Lymphoma ◽  
Case History ◽  
Clinical Picture ◽  
Clinical Relevance ◽  
Clinical Observation ◽  
Incidental Finding ◽  
Endoscopic Imaging ◽  
Biopsy Material ◽  
History Of

Clinical relevance. Duodenal MALT-lymphoma, a rare disease of the duodenum with a blurred clinical picture, frequently is an incidental finding at esophagogastroduodenoscopy. Therefore, the authors presented a clinical observation of a 59-yearold patient, whose diagnosis was established on the basis of endoscopic imaging, morphological and immunohistochemical investigations of biopsy material.The purpose of the study was to demonstrate clinical observation of MALT-lymphoma of duodenumMaterials and methods: The case history of a 59-year-old patient diagnosed with duodenal MALT-lymphoma is presented.

scholarly journals Therapeutic and diagnostic algorithm for colon lipoma

2021 ◽  
Vol 1 (5) ◽  
pp. 101-103
Author(s):  
I. Yu. Korzheva ◽  
N. E. Chernekhovskaya ◽  
E. V. Galaeva ◽  
N. V. Vychuzhanina ◽  
E. A. Khoreva
Keyword(s):  
Intestinal Obstruction ◽  
Clinical Features ◽  
Case History ◽  
Clinical Relevance ◽  
Clinical Case ◽  
Clinical Observation ◽  
Diagnostic Algorithm ◽  
Morphological Examination ◽  
History Of ◽  
Colonic Lipoma

Clinical relevance: Colon lipomas are not rare tumors, but they occur with blurred clinical features and patients arrive with complications- obstructive intestinal obstruction or bleeding. In this regard, the authors presented a clinical case of a 57-yearold patient whose diagnosis was established only by morphological examination of the surgical material.The purpose of the study was to demonstrate clinical observation of colon lipoma.Materials and methods: The case history of a 57-year-old patient diagnosed with colonic lipoma is presented.

scholarly journals CLINICAL OBSERVATION OF THE PATIENT WITH WEGENER'S GRANULOMATOSIS

2017 ◽  
Vol 1 (66) ◽  
pp. 89-97
Author(s):  
Валерий Войцеховский ◽  
Valeriy Voytsekhovskiy ◽  
Марина Погребная ◽  
Marina Pogrebnaya ◽  
Николай Гоборов ◽  
...  
Keyword(s):  
Clinical Picture ◽  
Wegener’S Granulomatosis ◽  
Clinical Observation ◽  
Wegener's Granulomatosis ◽  
Tracheobronchial Tree ◽  
Acute Onset ◽  
Upper Respiratory Tract ◽  
Biopsy Material ◽  
Adequate Treatment ◽  
Upper Respiratory

A brief review of the literature is devoted to the peculiarities of the clinical picture, diagnosis and treatment of Wegener's granulomatosis. The clinical observation of the patient with Wegener's granulomatosis is made from the personal practice of the authors. A complex differential diagnosis was made between pneumonia of different etiology, tuberculosis, lung cancer and granulomatous disease. Taking into account anamnesis and clinical picture of the disease (acute onset with fever, arthralgia, nasal and oral mucosa damage, lungs, kidneys, Raynaud's syndrome, hemorrhagic eruptions, digital vasculitis), histological examination of transbronchial lung tissue biopsy material diagnosed: Wegener's granulomatosis, a generalized form, with the lesions of the upper respiratory tract, tracheobronchial tree, lungs, heart, kidneys, an acute course. Despite adequate treatment, the disease progressed with the addition of various complications, and a lethal outcome was ascertained.

MALT lymphoma and eosinophilic oesophagitis: incidental finding— review of possible factors influencing the aetiopathogenesis of eosinophilic oesophagitis

2021 ◽  
Vol 14 (3) ◽  
pp. e239980
Author(s):  
Beatriz Fernandez Manso ◽  
Josefa Barrio Torres ◽  
Beatriz Martinez Escribano ◽  
Cristina Perez Fernandez
Keyword(s):  
Malt Lymphoma ◽  
Milk Protein ◽  
Sublingual Immunotherapy ◽  
Incidental Finding ◽  
Gastric Malt Lymphoma ◽  
Food Impaction ◽  
Eosinophilic Oesophagitis ◽  
High Proton ◽  
History Of ◽  
H Pylori

An 11-year-old boy with a history of atopy and allergic rhinitis under treatment with sublingual immunotherapy was referred following several episodes of food impaction. Diagnosis of eosinophilic oesophagitis, chronic gastritis and gastric mucosa-associated lymphoid tissue (MALT) lymphoma associated to Helicobacter pylori were confirmed. Results of the extension study were negative and the lymphoma was resolved with eradicating treatment for H. pylori. No improvement was observed in the oesophagitis after the withdrawal of immunotherapy and treatment with high proton pump inhibitor doses or following the omission of several foods to which subclinical sensitisation was confirmed. Oesophagitis was finally resolved by removing cow's milk protein. After 10 years, neither eosinophilic oesophagitis nor MALT lymphoma was observed.Gastric MALT lymphoma associated to H. pylori is a rare disorder in children. Although coexisting H. pylori infection is common in patients with eosinophilic oesophagitis, the association of gastric MALT lymphoma with eosinophilic oesophagitis has not been reported before.

scholarly journals Urethral Caruncle Presented as Premature Menarche in a 4-Year-Old Girl

2018 ◽  
Vol 2018 ◽  
pp. 1-2 ◽  
Author(s):  
Manori Gamage ◽  
D. Beneragama
Keyword(s):  
Postmenopausal Women ◽  
Case History ◽  
Vaginal Bleeding ◽  
Incidental Finding ◽  
Surgical Excision ◽  
Urethral Meatus ◽  
Young Girls ◽  
History Of ◽  
Acute Retention

Urethral caruncle (UC) is a benign fleshy outgrowth at the urethral meatus. It was first described by Samuel Sharp in 1750 and occurs mainly at the posterior lip of the urethra, and the exact aetiology is still uncertain. More often it was seen in the postmenopausal women, and only few cases are reported in young girls. Patients may be asymptomatic and could find this as an incidental finding or they may present with symptoms such as dysuria, bleeding per vagina, haematuria, a mass protruding through vagina, and acute retention of urine. Here, we report the case history of a 4-year-old girl presented with vaginal bleeding which was taken as she has attended menarche and found to have urethral caruncle which was the cause for bleeding. Histology confirmed the diagnosis, and girl was completely cured following surgical excision.

scholarly journals Extra-Abdominal Fibromatosis: A Case Report

2003 ◽  
Vol 82 (4) ◽  
pp. 322-325
Author(s):  
Nathan Stephens ◽  
Farhan Ahsan ◽  
Daran P. Murray ◽  
Akhtar Hussain ◽  
Andrea D. Chapman
Keyword(s):  
Case Report ◽  
Head And Neck ◽  
Rare Disease ◽  
Clinical Picture ◽  
Rapid Growth ◽  
Current Opinion ◽  
History Of ◽  
Painless Mass

Head and neck fibromatosis is a rare disease with a variable clinical picture. We report the case of a 40-year-old woman who had a 1-week history of a painless mass overlying her right neck. Histology confirmed a diagnosis of extra-abdominal fibromatosis. Two unusual features of this case were the site of the lesion and its rapid growth. In this article, we discuss the clinical picture of head and neck fibromatosis, its etiology and pathology, and current opinion regarding its treatment.

scholarly journals The problems of clinical and epidemiological basis of diagnosis of rabies in the example of case history observation

2016 ◽  
Vol 21 (4) ◽  
pp. 211-218
Author(s):  
V. V Nikiforov ◽  
Valery A. Malov ◽  
N. V Trusova
Keyword(s):  
Differential Diagnosis ◽  
Rabies Virus ◽  
Clinical Diagnosis ◽  
Case History ◽  
Clinical Picture ◽  
Clinical Observation ◽  
Human Infection ◽  
Review Of The Literature ◽  
Mucous Membranes ◽  
Special Studies

In the article there is considered the clinical observation with a rare mechanism of human infection with rabies virus from a home decorative dog through the salivation of the mucous membranes and throat while caring for a dying animal. The diagnosis of rabies in the dead dog was established retrospectively after its exhumation and special studies. There is analyzed the dynamics of the clinical picture of rabies in human for the purpose of differential diagnosis and substantiation of clinical diagnosis. There is presented a brief review of the literature.

scholarly journals From edematous syndrome to the diagnosis of "intestinal lymphangiectasia" (clinical observation of a rare disease)

2018 ◽  
Vol 42 (4) ◽  
pp. 66-72
Author(s):  
N. B. Gubergrits ◽  
K. Y. Linevskaya ◽  
K. A. Voronin
Keyword(s):  
Rare Disease ◽  
Clinical Picture ◽  
Clinical Observation ◽  
Intestinal Lymphangiectasia ◽  
Diagnostic Approaches

The article presents differential diagnostic approaches to the verification of intestinal lymphangiectasia in a patient with edematous syndrome; features of the clinical picture, diagnosis, treatment and prognosis of intestinal lymphangiectasia are shown.

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