scholarly journals Recurrent Rash Secondary to Shiitake Dermatitis

2021 ◽  
Vol 8 (3) ◽  
Author(s):  
Nguyen L ◽  
◽  
Prodanovic E ◽  
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Clinical Features ◽  
Relevant Literature ◽  
Cutaneous Reaction ◽  
Shiitake Mushrooms ◽  
Cutaneous Reactions

Ingestion of shiitake mushrooms can result in a cutaneous reaction known as shiitake dermatitis. In this case report, a recurrent rash in a 56-yearold female patient was found to be shiitake dermatitis. The clinical features, histology, and relevant literature are discussed in the context of differentiating shiitake dermatitis from other similar cutaneous reactions.

scholarly journals EFFECTIVE MANAGEMENT OF VATALA YONIVYAPDA W.S.R ENDOMETRIOSIS BY AYURVEDA: A CASE REPORT

2021 ◽  
Vol 9 (9) ◽  
pp. 2271-2278
Author(s):  
Poonam Kumari ◽  
Poonam Choudhary ◽  
Hetal H. Dave ◽  
Sonu Sonu
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Clinical Features ◽  
Chief Complaint ◽  
Complete Relief ◽  
Effective Management ◽  
Present Patient ◽  
Unbearable Pain ◽  
Laboratory Investigations ◽  
Extreme Pain

Background: A married Hindu female patient of 44 years of age visited OPD of National Institute of Ayurveda, deemed to be university, Jaipur on 30 December 2020. She was having chief complaint of extreme and unbearable pain starting 2-3 days before menstruation and continuing in her menstruation also. Methodology: On reviewing her laboratory investigations (USG) she was diagnosed with Endometriosis. On de- tailed history, Dosha assessment was done based on the clinical features and mainly Vata Dosha was found to be vitiated in the present patient. Considering this, she was diagnosed with Vatala Yonivyapada, and treatment was given to her based on the line of treatment explained for Vatala Yonivyapada in classics. Result: Patients showed complete relief in extreme pain during menstruation in the very 1st first cycle following treatment and she is having complete relief in pain to date. Keywords: Vatala Yonivyapada, Endometriosis, Dysmenorrhea

Gingival Tumor in Young Female Patient: A Case Report

2021 ◽  
Vol 6 (1) ◽  
Author(s):  
Namala A ◽  
◽  
Halerolli D ◽  
Poonja PA ◽  
Rao PK ◽  
...  
Keyword(s):  
Case Report ◽  
Periodontal Disease ◽  
Female Patient ◽  
Clinical Sign ◽  
Clinical Features ◽  
Oral Hygiene ◽  
Young Female ◽  
Clinical Concern ◽  
Gingival Enlargement

Alteration in size of gingiva is one of the clinical features of periodontal disease. Increase in size of gingiva, which is termed as gingival enlargement or gingival over growth is a common clinical sign of gingival disease and a matter of great clinical concern. Increase in size alters the physiologic contour of gingiva, creates areas of plaque accumulation, intereferes with regular oral hygiene procedures, and creates aesthetic problems. In severe cases, it interefere with mastication and phonation. Enlargement may involve one or more components of gingiva. Depending on the involvement of components of gingiva and distribution, gingival enlargement can be Localized, genaralized and marginal, papillary, diffuse and discrete. Depending on etiology and pathogenesis, it can be classified as inflammatory enlargement, fibrotic enlargement, combined enlargement, enlargement associated with systemic conditions, neoplastic enlargement and false enlargements.

Intramedullary inclusion cysts of the cervicothoracic junction

2007 ◽  
Vol 7 (2) ◽  
pp. 236-242 ◽  
Author(s):  
Alfred T. Ogden ◽  
Alexander G. Khandji ◽  
Paul C. McCormick ◽  
Michael G. Kaiser
Keyword(s):  
Spinal Cord ◽  
Case Report ◽  
Surgical Treatment ◽  
Dermoid Cyst ◽  
Clinical Features ◽  
Epidermoid Cyst ◽  
Relevant Literature ◽  
Literature Discussion ◽  
Cervicothoracic Junction

✓Intramedullary inclusion cysts are extremely rare within the rostral spinal cord. In this case report the authors outline the clinical features and surgical treatment of one dermoid cyst and one epidermoid cyst of the cervicothoracic junction. The authors also include a relevant literature discussion regarding the treatment and the embryological origin of these lesions.

scholarly journals The Role of Trichoscopy in Keratosis Follicularis Spinulosa Decalvans: Case Report and Review of the Literature

2020 ◽  
pp. 1-7
Author(s):  
Aurora Alessandrini ◽  
Giancarlo Brattoli ◽  
Bianca Maria Piraccini ◽  
Ambra Di Altobrando ◽  
Michela Starace
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Clinical Features ◽  
Diagnosis And Treatment ◽  
Skin Involvement ◽  
Review Of The Literature ◽  
Case Presentation ◽  
Keratosis Follicularis ◽  
Scarring Alopecia

<b><i>Introduction:</i></b> Keratosis follicularis spinulosa decalvans (KFSD) is a rare, X-linked, hereditary disorder of keratinization, characterized by skin involvement and progressive scarring alopecia of scalp, eyebrows, and eyelashes. The diagnosis is helped by the particular clinical features, but pathology is mandatory. <b><i>Case Presentation:</i></b> We described a case of a female patient referred to the outpatient’s hair consultation of our department, in which we performed trichoscopy as a very useful tool for the diagnosis, followed by pathology that confirmed KFSD. <b><i>Conclusion:</i></b> In our article, we underlined the importance of trichoscopy for the diagnosis of this hair disease, with also a review of the literature on diagnosis and treatment.

scholarly journals Foster Kennedy Syndrome: A Case Report

2021 ◽  
Vol 26 (4) ◽  
Author(s):  
Juan José Díaz-Vintimilla ◽  
Christian Méndez-González ◽  
Fabián Díaz-Heredia ◽  
Francisco Pérez-Allende ◽  
Diego Romero-Cano
Keyword(s):  
Visual Acuity ◽  
Case Report ◽  
Female Patient ◽  
Clinical Features ◽  
Optic Atrophy ◽  
Common Condition ◽  
Intracranial Mass ◽  
Foster Kennedy Syndrome ◽  
Visual Disturbances ◽  
Sphenoid Wing Meningioma

Foster Kennedy Syndrome is a classic, yet rare, neuro-ophthalmologic syndrome due to an intracranial mass, most often a tumor, that consists of optic atrophy on the same side of the lesion and contralateral papilledema. We present the case of a 48-year-old female patient with decreased visual acuity and the typical clinical features described above due to a sphenoid wing meningioma. Although not a common condition, Foster Kennedy Syndrome should always be kept in mind in a patient with visual disturbances secondary to an intracranial mass.

Terbutaline Concentrations in Self-Poisoning: A Case Report

1987 ◽  
Vol 6 (6) ◽  
pp. 525-526 ◽  
Author(s):  
A. Heath ◽  
B.-Å. Hultén
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Clinical Features ◽  
Plasma Concentrations ◽  
Young Female ◽  
Therapeutic Level

A young female patient was admitted twice within two months, each time after an overdose of 500 mg terbutaline. Clinical features included nausea, tachycardia, tremor, hyperglycemia and hypokalemia. Although plasma concentrations of terbutaline were at least 50 times the normal therapeutic level, after potassium substitution the outcome was uneventful.

scholarly journals Sclerosing encapsulating peritonitis secondary to dermoid cyst rupture: a case report

2011 ◽  
Vol 93 (5) ◽  
pp. e39-e40 ◽  
Author(s):  
SJ Fossey ◽  
JNL Simson
Keyword(s):  
Case Report ◽  
Dermoid Cyst ◽  
Female Patient ◽  
Clinical Features ◽  
Sclerosing Encapsulating Peritonitis ◽  
Encapsulating Peritonitis ◽  
Chemical Peritonitis ◽  
Cyst Rupture

This case report documents the presentation and management of a 26-year-old female patient diagnosed with SEP secondary to dermoid cyst rupture. The authors postulate that acute chemical peritonitis secondary to dermoid cyst rupture can develop into SEP resulting in the clinical features depicted in this case report.

scholarly journals Unusual association between cheilitis glandularis and actinic cheilitis.

2017 ◽  
Vol 74 (1) ◽  
pp. 74
Author(s):  
Juliana Tristão Werneck ◽  
Taiana Campos Leite ◽  
Ana Maria De Oliveira Miranda ◽  
Eliane Pedra Dias ◽  
Karin Soares Gonçalves Cunha ◽  
...  
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Clinical Features ◽  
Simultaneous Occurrence ◽  
Actinic Cheilitis ◽  
Patient Case ◽  
Lower Lip ◽  
Unusual Association ◽  
Special Concern ◽  
Malignancy Potential

Objective: our aim is to report the simultaneous occurrence of both diseases on the lower lip of a middle-aged female patient. Case Report: she presented clinical features compatible with cheilitis glandularis and actinic cheilitis, confirmed by histopathological exam. Conclusion: the importance of the present case is the rare concomitant occurrence of both conditions, with special concern towards the malignancy potential related to both diseases.

Ectodermal Dysplasia in two siblings: A Case report.

2019 ◽  
Author(s):  
CHAITHRA KALKUR ◽  
NILOFER HALIM ◽  
ANUSHA RANGARE ◽  
Rumisha .
Keyword(s):  
Case Report ◽  
Key Words ◽  
Clinical Features ◽  
Ectodermal Dysplasia ◽  
Heterogeneous Group ◽  
Eccrine Glands ◽  
Key Words Ectodermal Dysplasia

Ectodermal dysplasia is a heterogeneous group of inherited disorder affecting two or more ectodermally derived tissues such as skin, hair, nails, eccrine glands and teeth. The disorder is of two types: Hypohydrotic ectodermal dysplasia/Christ seimens –Touraine syndrome and Hydrotic ectodermal dysplasia/clousten syndrome. Commonly associated signs include hypohidrosis, anomalous dentition, onychodysplasia, hypotrichosis. Multidisciplinary approaches are required for optimal treatment3. Here, we present two cases of 19 and 13 year old male siblings who were diagnosed with the disorder based upon their clinical features. Key Words: ectodermal dysplasia, hypodontia; anomalous dentition.

Healing Of A Large Osteolytic Mandibular Lesion – A Case Report

2018 ◽  
Author(s):  
Ingrid Różyło-Kalinowskav ◽  
Karolina Sidor
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Surgical Approach ◽  
Orthodontic Treatment ◽  
Incidental Finding ◽  
Osteolytic Lesion ◽  
Panoramic Radiograph ◽  
Endodontic Treatment ◽  
Osteolytic Lesions

The purpose of this article was to present a case report of 11–year old female patient with a large osteolytic mandibular lesion which healed after endodontic treatment. The patient was referred for radio diagnostics due to an incidental finding of a large osteolytic lesion of the area of the left lower first and second premolars in the panoramic radiograph taken before orthodontic treatment. CBCT was performed and the patient asked to have teeth 33-35 treated by endodontics before surgery. The patient missed the surgical appointment and when she reappeared several months later, the lesion showed signs of healing thus surgery were aborted. The presented case testifies to the observation that even large osteolytic lesions can heal after endodontic treatment without surgical approach.

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