scholarly journals CLINICAL CASE OF GENERAL SOMATIC COMPLAINTS IN 47 Y.O. FEMALE

2018 ◽  
Keyword(s):  
Uterine Fibroid ◽  
Clinical Case ◽  
Somatic Complaints ◽  
General Character ◽  
General Weakness

A clinical case of general somatic complaints in 47 y.o. female, presenting for several years has described. Patient F., presents with uncertain complaints of general character – tiredness, general weakness, loss of energy. During the biennium was examined and treated by gynecologist, endocrinologist, cardiologist, gastroenterologist with no benefit. Anamnesis vita is significant for uterine fibroid. After thorough interviewing was found that patient was done ECG, EchoCG, gastroscopy, thyroid tests but no CBC, urinalysis, general biochemical panel during this two years. The CBC results were stunning and gave answers to all questions.

scholarly journals Familial adenomatous colorectal polyposis complicated by colonic obturation: a clinical case

2020 ◽  
Vol 27 (6) ◽  
pp. 175-185
Author(s):  
V. M. Durleshter ◽  
A. A. Kryachko ◽  
K. D. Chuguzov ◽  
M. K. Tarlanova
Keyword(s):  
Intestinal Obstruction ◽  
Clinical Case ◽  
Rare Complication ◽  
Clinical Manifestations ◽  
Right Hemicolectomy ◽  
Stage Ii ◽  
Clinical Group ◽  
Colorectal Polyposis ◽  
General Weakness ◽  
Group 2

Background. Colorectal obturation is a fairly rare complication in patients with colorectal polyposis. Case descriptions of colonic obturation with underlying familial adenomatous colorectal polyposis have not been reported to date in national and foreign literature.Clinical Case Description. Patient G., female, 31 yo, was emergently admitted to a surgical unit with a preliminary diagnosis: acute intestinal obstruction, complaints of abdominal pain, nausea, vomiting, stool and gas outlet blockage, marked general weakness. Clinical and biochemical blood tests without peculiarities. Signs of intestinal obstruction in abdominal ultrasonic and X-ray examination. Obstructive right hemicolectomy performed as emergent surgery. Diagnosis: transverse colonic C-r T3NoMo, stage II, clinical group 2. Patient had routine fibrocolonoscopy in six months; polyps were revealed in all operated colon portions. APC genetic test was positive, total colectomy was decided with single-barrel ileostomy excretion on anterior abdominal wall. Definitive diagnosis: transverse colonic C-r T3NoMo, stage II, developed with underlying familial adenomatous colorectal polyposis, clinical group 2.Conclusion. Diagnosis of familial adenomatous colorectal polyposis with acute intestinal obturation is challenging due to forced urgent surgical intervention and lack of time for a detailed deeper examination in avoidance of baleful consequences. The case reported demonstrates that clinical manifestations of familial adenomatous colorectal polyposis extend beyond the routine complaints of abdominal bloating, stool blockage and rectal bleeding towards a formidable complication of acute colonic obturation of polypoid genesis.

scholarly journals Skene Keith. Total disappearance of a fibroid tumor after D-r Apostoli’s treatment. (Brit. Med. Journ. July 9, 1892). Complete disappearance of fibrous tumor after treatment according to the Apostoli method.

2020 ◽  
Vol 7 (2) ◽  
pp. 185-186
Author(s):  
F. Kuhn
Keyword(s):  
Uterine Fibroid ◽  
Menstrual Period ◽  
Complete Disappearance ◽  
Time Increase ◽  
Lower Abdomen ◽  
Only Child ◽  
Constant Pain ◽  
General Weakness ◽  
Fibrous Tumor ◽  
Total Disappearance

Diagnosis of uterine fibroid was made on the basis of the following data: N.N., 29 years old, since the birth of her only child, who is now 10 years old, has never felt completely well. General weakness, dysmenorrhoea; pains for the period of regulation with each time increase; Months are becoming more and more abundant, both in quantity and in duration: in every period of the menstrual period, she spends from 50-70 napkins. At the first visit of the author, in July 1889, the patient walked from weakness with difficulty, complaining of constant pain in the lower abdomen. Upon examination, it was found that the pelvis was filled with a fibrous tumor of the uterus.

scholarly journals Skeletal muscle damage in the course of coronavirus disease (COVID-19) in a pediatric practice. Own supervision: a clinical case

2021 ◽  
Vol 17 (7) ◽  
pp. 11-15
Author(s):  
V.O. Svystilnyk ◽  
O.S. Mihnusheva ◽  
K.B. Savinova
Keyword(s):  
Skeletal Muscle ◽  
Muscle Damage ◽  
Acute Phase ◽  
Clinical Case ◽  
Clinical Symptoms ◽  
Pathological Condition ◽  
Connective Tissue Diseases ◽  
Skeletal Muscle Damage ◽  
General Weakness ◽  
The Right

Background. Coronavirus disease (COVID-19) pandemic is still at the heart of healthcare in Ukraine and over the world. The nervous system and other human organs and systems can be affected by pathogenic nature of SARS-CoV-2. We purposed to pay physicians’ attention to the diagnosis of skeletal muscle damage, in particular rhabdomyolysis, to avoid possible complications in COVID-19. Materials and methods. We have examined a group of children with skeletal muscle damage on the background of COVID-19 during 2020–2021. A clinical case from own practice has been presented in the article. Results and conclusions. The patient, a 15-year-old boy, developed general weakness, severe pain in the right thigh and hip joint, fever 33 days after the acute phase of coronavirus disease. The differential diagnosis was carried out between skeletal muscle damage and osteomyelitis. Diffuse connective tissue diseases, oncohematological disorders, and hepatitis were excluded on the basis of clinical data and examinations. The inflammatory changes in m.iliopsoas, m.obturatorius internus and m.piriformis with abscess formation identified during clinical examination and magnetic resonance imaging, along with high levels of blood transaminases indicated the development of rhabdomyolysis. The detected positive IgG to SARS-CoV-2 confirmed the association of this pathological condition with the previous acute phase of COVID-19. Signs of coagulopathy, anemia in the hemogram simultaneously with the clinical symptoms of rhabdomyolysis confirmed the systemic lesions in the course of coronavirus disease in the child. Timely assessment of clinical symptoms (general weakness, muscle pain) and levels of creatine phosphokinase, transaminases, electrolytes, creatinine, blood urea will help make an early diagnosis of rhabdomyolysis, prescribe adequate therapy and prevent the deve-lopment of severe complications.

scholarly journals Gaucher's disease

2021 ◽  
pp. 147-154
Author(s):  
R. G. Saifutdinov ◽  
R. R. Akhunova ◽  
A. A. Kurshakov ◽  
E. I. Mitusheva ◽  
R. R. Saifutdinov ◽  
...  
Keyword(s):  
Clinical Case ◽  
Hereditary Disease ◽  
Gaucher's Disease ◽  
Gaucher’S Disease ◽  
Surgical Department ◽  
General Weakness ◽  
Difficulty Breathing ◽  
Lysosomal Accumulation ◽  
Genetic Examination ◽  
Rupture Of The Spleen

The article presents a rare clinical case of Gaucher's disease, a hereditary disease that belongs to lysosomal accumulation diseases. A 36-year-old patient was admitted to the clinic with complaints of pain in the left half of the abdomen, pain in the chest, cough with yellow sputum, difficulty breathing due to pain, general weakness. The mental underdevelopment, hepatosplenomegaly, anemia, thrombocytopenia, and the threat of rupture of the spleen were revealed in the process of collecting anamnesis and examination. The patient was transferred to the surgical department, and a splenectomy was performed. Histological examination of the spleen and genetic examination confirmed the diagnosis of Gaucher's disease.

scholarly journals Urticaria-like rash in a patient with COVID-19 associated pneumonia of moderate severity: aspects of pathogenesis

2020 ◽  
Vol 23 (2) ◽  
pp. 109-114
Author(s):  
Ekaterina V. Orlova ◽  
L. M. Smirnova ◽  
N. I. Melikova ◽  
K. Yu. Popova
Keyword(s):  
Clinical Case ◽  
Case Reports ◽  
Clinical Manifestations ◽  
Skin Lesions ◽  
Infection Process ◽  
Moderate Severity ◽  
Skin Manifestations ◽  
General Weakness

In mid 2020, the number of new coronavirus (COVID-19) cases has exceeded globally six million. The clinical manifestations of COVID-19 infection are numerous mostly causing damage to the bronchopulmonary system in the form of a dry cough, rhinitis, dyspnea, fever, myalgia, and general weakness. Skin manifestations of COVID-19 are rare and currently include five types of skin lesions occurring during the infection process, which are reliably recorded in only a limited number of case reports and certain analytical publications. This article describes the clinical case of a 28-year-old patient with urticaria-like disseminated rash and confirmed COVID-19-associated pneumonia.

scholarly journals Case report of the successful uterine fibroid embolization via transradial approach

2015 ◽  
Vol 64 (4) ◽  
pp. 99-102
Author(s):  
Evgeny Rafailovich Khayrutdinov ◽  
Ivan Mikhaylovich Vorontsov ◽  
Olga Yurievna Tsygankova ◽  
Elena Nikolaevna Kravchenko ◽  
Yuriy Timofeevich Ignatiev ◽  
...  
Keyword(s):  
Case Report ◽  
Uterine Fibroid ◽  
Clinical Case ◽  
Transfemoral Approach ◽  
Technical Aspects ◽  
Uterine Fibroid Embolization ◽  
Transradial Approach

We represent the first clinical case of the successful uterine fibroid embolization via transradial approach. The technical aspects and the main advantages of this type of the procedure compared to the uterine fibroid embolization via transfemoral approach are described.

Ovarian and uterine leiomyosarcoma: which one is the primary?

2019 ◽  
Vol 0 (0) ◽  
Author(s):  
Mohamad Nasir Shafiee ◽  
Chew Kah Teik ◽  
Reena Rahayu Md Zain ◽  
Nirmala Kampan
Keyword(s):  
Uterine Fibroid ◽  
Clinical Case ◽  
Uterine Leiomyosarcoma

Abstract Uterine leiomyosarcoma (LMS) is rare but primary ovarian LMS is even rarer constituting less than 0.1% of all gynecologic disorders. Neither histologic features nor immunohistochemistry could be utilized to distinguish between uterine or ovarian origin. We illustrate a clinical case of metastatic LMS to the ovary in a woman with underlying uterine fibroid presenting with anemia with heavy menses.

2.2. Working Group 2: Conceptual Definitions of Reference Coordinate Systems for Earth Dynamics

1975 ◽  
Vol 26 ◽  
pp. 21-26
Keyword(s):  
Coordinate System ◽  
Working Group ◽  
General Character ◽  
Coordinate Systems ◽  
Reference Coordinate System ◽  
Group 2 ◽  
Definition Of ◽  
Earth Dynamics

An ideal definition of a reference coordinate system should meet the following general requirements:1. It should be as conceptually simple as possible, so its philosophy is well understood by the users.2. It should imply as few physical assumptions as possible. Wherever they are necessary, such assumptions should be of a very general character and, in particular, they should not be dependent upon astronomical and geophysical detailed theories.3. It should suggest a materialization that is dynamically stable and is accessible to observations with the required accuracy.

The Variable Nature of Stuttering: A Clinical Case Study

1995 ◽  
Vol 22 ◽  
pp. 29-35
Author(s):  
Jennifer Gutierrez ◽  
Anthony Caruso
Keyword(s):  
Clinical Case ◽  
Clinical Case Study ◽  
Variable Nature
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