scholarly journals A Sarcoidosis Case With Galaxy Sign Admitted With A Rare Symptom : Hemoptysis

2020 ◽  
pp. 476-481
Author(s):  
Lale SERTÇELİK ◽  
Fatma ARMAĞAN HAZAR
Keyword(s):  
Rare Symptom

CAN SNEEZING BE A RARE SYMPTOM OF NAZOPALATINE CYST?

2016 ◽  
Author(s):  
Nuray Yılmaz Altintas
Keyword(s):  
Rare Symptom

scholarly journals Supernumerary phantom limb as a rare symptom of epileptic seizures-case report and literature review

Epilepsia ◽  
2011 ◽  
Vol 52 (8) ◽  
pp. e97-e100 ◽  
Author(s):  
Alban Millonig ◽  
Thomas Bodner ◽  
Eveline Donnemiller ◽  
Elisabeth Wolf ◽  
Iris Unterberger
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Epileptic Seizures ◽  
Phantom Limb ◽  
Supernumerary Phantom Limb ◽  
Rare Symptom

scholarly journals Retenção Urinária Como Manifestação de Hematocolpos

2020 ◽  
Vol 33 (13) ◽  
Author(s):  
Íris Santos Silva ◽  
Renata Martello ◽  
António Mendes ◽  
Albertino Chaves
Keyword(s):  
Emergency Department ◽  
Abdominal Pain ◽  
Case Report ◽  
Urinary Retention ◽  
Genital Tract ◽  
Rare Condition ◽  
Tanner Stage ◽  
Imperforate Hymen ◽  
Uncommon Condition ◽  
Rare Symptom

Hematocolpos is an obstruction of the menstrual flow due to an anomaly of the genital tract, with imperforate hymen being the most common one. It is an uncommon condition, with a prevalence of 1:1000 – 1:16 000. It is usually an asymptomatic condition until the onset of menarche, when there is accumulation of blood in the vagina (hematocolpos) or in the uterus (hematometra). A rare symptom of hematocolpos could be urinary retention. Our case report is about a 12-year-old girl, with no menarche and Tanner stage M4/P5, who was admitted to our emergency department with abdominal pain and urinary retention. A brief review of this rare condition is presented, in order to remind clinicians about its existence, so that it can be diagnosed and treated as quickly as possible.

The Reflection of Lilliputian Hallucinations in Paintings of a Schizophrenic Patient

2011 ◽  
Vol 26 (S2) ◽  
pp. 1379-1379
Author(s):  
F. Estilaee ◽  
A. Ghaffari Nejad
Keyword(s):  
Mental Disorders ◽  
Schizophrenic Patient ◽  
Van Gogh ◽  
The Real ◽  
Paul Gauguin ◽  
Real Size ◽  
Rare Symptom

Since several years ago the relation between art and mental disorders has been interesting for psychiatrists. This relation has more importance when understanding famous painters such as Van Gogh, Paul Gauguin and Louis Wain have had such disorders.Psychotic patients may project their symptoms into their drawings and use paintings as a way to illustrate their special feelings and thoughts. Without them understanding patient’s world and their symptoms is impossible.When hallucinations are too amazing to believe and more persecutor than any pain, and when thoughts are so dispersed which other cannot understand and nevertheless, there is no treatment for these boring symptoms, art and specially painting may be a way to relief them.Lilliputian hallucination is a rare symptom in psychotic patients; a visual type hallucination that things and persons appears smaller than the real size. Patients usually describe them as the persecutor dwarfs or life from another world.Here we introduce a schizophrenic patient with Lilliputian hallucination who created famous paintings. In these paintings, patient was drawn dwarfs in nearly one inch. They are creatures between man and mouse, sometimes whisper and occasionally walk on his head or body.

Enuresis as a rare symptom of the dystopic spleen in a child

1999 ◽  
Vol 158 (10) ◽  
pp. 870-871 ◽  
Author(s):  
A. Kapellerová ◽  
J. Siman ◽  
J. Rašková ◽  
V. Cingel ◽  
D. Haviar
Keyword(s):  
Rare Symptom

Contribution to the Dressing Disability As a Focal Sign and to the Imperception Phenomena

1948 ◽  
Vol 94 (396) ◽  
pp. 611-622 ◽  
Author(s):  
R. E. Hemphill ◽  
R. Klein
Keyword(s):  
Head Injury ◽  
Detailed Analysis ◽  
Brain Lesions ◽  
Cerebral Hemispheres ◽  
Mental Condition ◽  
Rare Symptom

Inability to dress oneself is a rare symptom in focal brain lesions. We have observed it in two cases, a tumour expanding between the cerebral hemispheres, and a case of head injury in which the mental condition was sufficiently intact to allow a detailed analysis: In discussing the imperception phenomena of the tumour case, we have referred to certain others of relevant interest.

Gynecomastia as a rare symptom in ß-HCG-positive giant-cell tumor of bone GCTOB.

2015 ◽  
Vol 33 (15_suppl) ◽  
pp. e21501-e21501
Author(s):  
Arp Klaus Blum
Keyword(s):  
Giant Cell Tumor ◽  
Giant Cell ◽  
Cell Tumor ◽  
Rare Symptom

scholarly journals Allergenic activity of honey

2012 ◽  
Vol 59 (1) ◽  
pp. 257-263
Author(s):  
Bogdan Kędzia ◽  
Elżbieta Hołderna-Kędzia
Keyword(s):  
Grass Pollen ◽  
Digestive System ◽  
Bee Venom ◽  
Food Components ◽  
Allergenic Activity ◽  
The Cross ◽  
Rare Symptom

An allergy to honey is a rare symptom. It usually occurs when people are allergic to food components, pollen and bee venom. Most often an allergy to honey is manifested by disturbances of skin and digestive system. Anaphylaxis is seldom, pollen proteins are more often the cause of an allergy to honey than honeybee ones. In particular cases an allergy can be caused by moulds, yeasts and secretion of sapsucking insects. An allergy to honey is often caused by pollen of floral plants from Compositae family (e.g.: sunflower, mugwort, marguerite, dandelion, golden rod, ragweed). It is caused more rarely by grass pollen (timothy) and trees (birch, hazel, olive). The cross allergy between two kinds of pollen of the same family (dandelion and sunflower) and between pollen of different families (sunflower and celery) is well-known. On this basis one can consider that the allergy to one monofloral honey can cause the allergy to other monoflower ones.

scholarly journals AUTOIMMUNE MYELOFIBROSIS ASSOCIATED WITH SYSTEMIC LUPUS ERYTHEMATOSUS: EXCEPTIONALLY RARE OR UNDERRECOGNIZED?

2021 ◽  
Vol 2 (2) ◽  
pp. 96-100
Author(s):  
Döndü Üsküdar Cansu ◽  
Cengiz Korkmaz
Keyword(s):  
Systemic Lupus Erythematosus ◽  
Bone Marrow ◽  
Lupus Erythematosus ◽  
Case Reports ◽  
Classification Criteria ◽  
Systemic Lupus ◽  
Organ Systems ◽  
Hematological Abnormalities ◽  
Chronic Autoimmune Disease ◽  
Rare Symptom

Systemic lupus erythematosus (SLE) is a chronic autoimmune disease which may involve several organs or organ systems. SLE may also have hematological as well as joint, kidney, and central nervous system involvements. Hematological abnormalities such as anemia, leukopenia, thrombocytopenia, and autoimmune hemolytic anemia are the best-known and most common hematological findings detected in SLE patients which are included in the classification criteria for SLE.  Autoimmune myelofibrosis (AIMF) refers to bone marrow (BM) fibrosis (myelofibrosis) that develops in an autoimmune setting. Myelofibrosis is not among the SLE classification criteria and it is also not well-known. Current reports in the literature on SLE-associated AIMF are mostly restricted to case reports or reviews of such case reports. The occurrence of BM fibrosis in SLE patients has been explored merely in few studies which concluded that myelofibrosis is a rare symptom of SLE. Herein, we propose the hypothesis that SLE-associated AIMF is not rare and, on the contrary, it can indeed be more frequent than what is known or expected.

scholarly journals Vomer Agenesis as a Rare Cause of Hypernasality

2018 ◽  
Vol 5 ◽  
Author(s):  
Adam Mohamad ◽  
Rohaida Ibrahim ◽  
Khairul Azhar Mohd Rajet ◽  
Irfan Mohamad ◽  
Anura Aman
Keyword(s):  
Cleft Palate ◽  
Surgical Complication ◽  
Nasolacrimal Duct ◽  
Neuromuscular Disorder ◽  
Velopharyngeal Insufficiency ◽  
Air Emission ◽  
Submucous Cleft Palate ◽  
Cleft Palate Repair ◽  
Palate Repair ◽  
Rare Symptom

Hypernasality which is rare symptom commonly occur as a consequence of velopharyngeal insufficiency (VPI). VPI usually manifested as nasal air emission and hypernasal resonance during speech. The cause can be divided into congenital, neuromuscular disorder and surgical complication. Congenital cause of VPI includes cleft palate, nasal septum malformation such as vomer agenesis, submucous cleft palate and velar dysplasia, while neuromuscular VPI can be due to cerebral palsy or cerebrovascular accident. Surgical cause of VPI could be due to adenoidectomy and scarring of the velum post palatoplasty in cleft palate repair. We present a 17-year-old man who was diagnosed of congenital left nasolacrimal duct obstruction referred to us for left endoscopic dacrocystorhinostomyin which during nasoendoscopic examination revealed absence of vomer.

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