Visita domiciliar: nova nuance frente a pandemia de Covid 19 - relato de experiência / Home visit: a new nuance in the face of the Covid 19 pandemic - case report

Beta-hemolytic Streptococcus group G, a rare human pathogen, has long been implicated in human disease as causing pharyngitis, puerperal sepsis, empyema, and even septicemia. We are reporting a rare, life-threatening, acute illness, primary peritonitis, due to this organism, whose etiological source probably was a family dog. Case Report R.K., a 2-year-old girl, was admitted with the complaints of anorexia, vomiting of three days' duration, and severe abdominal distension of one day's duration. The symptoms started following a burn injury over the face and lips three days prior to admission. Past history was noncontributory. Physical examination revealed an ill child of average size, fully conscious.

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Bilateral Sturge Weber Syndrome- a rare case report

Nepalese Journal of Ophthalmology ◽

10.3126/nepjoph.v5i1.7841 ◽

2013 ◽

Vol 5 (1) ◽

pp. 129-132 ◽

Cited By ~ 1

Author(s):

P Singh ◽

S Singh

Keyword(s):

Case Report ◽

Rare Case ◽

Unusual Case ◽

The Other ◽

Advanced Stage ◽

Weber Syndrome ◽

Rare Case Report ◽

The Face ◽

Bilateral Condition ◽

Sturge Weber Syndrome

Background: Sturge-Weber syndrome is a rare congenital neuro- oculo- cutaneous disorder. Objective: To report a very rare unusual case of bilateral manifestation of Sturge Weber syndrome. Case: We report an unusual case of a 17-year-old female with advanced stage of bilateral glaucoma associated with facial nevus extending to the other half of the face as well and bilateral intracranial calcification. Conclusion: Sturge -Weber syndrome can manifest as a bilateral condition. Nepal J Ophthalmol 2013; 5(9):129-132 DOI: http://dx.doi.org/10.3126/nepjoph.v5i1.7841

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Solitary neurofibroma of the face masquerading as a low-flow vascular malformation – case report and experience of management

JPRAS Open ◽

10.1016/j.jpra.2018.12.003 ◽

2019 ◽

Vol 19 ◽

pp. 67-72 ◽

Cited By ~ 1

Author(s):

Stephen R Ali ◽

Susan A Hendrickson ◽

Graham Collin ◽

Jon Oxley ◽

Robert P Warr

Keyword(s):

Case Report ◽

Vascular Malformation ◽

Low Flow ◽

Solitary Neurofibroma ◽

The Face

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Regional spread of cutaneous squamous cell carcinoma of the face via facial vein tumor thrombus: a case report

American Journal of Otolaryngology ◽

10.1016/j.amjoto.2007.10.007 ◽

2008 ◽

Vol 29 (6) ◽

pp. 423-425 ◽

Cited By ~ 1

Author(s):

Aysenur Meric Teker ◽

Robert R. Lorenz ◽

Walter T. Lee ◽

Aaron Hoschar

Keyword(s):

Squamous Cell Carcinoma ◽

Case Report ◽

Cell Carcinoma ◽

Squamous Cell ◽

Tumor Thrombus ◽

Cutaneous Squamous Cell Carcinoma ◽

Facial Vein ◽

The Face

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Solitary Trichoepithelioma of Nose: A Rare Case Report and Review of Literature

International Journal of Head and Neck Surgery ◽

10.5005/jp-journals-10001-1237 ◽

2015 ◽

Vol 6 (3) ◽

pp. 115-117

Author(s):

Sachin Lal Shilpakar ◽

Bivek Aryal ◽

Shyam Thapa Chettri ◽

Apar Pokharel ◽

Deepak Paudel

Keyword(s):

Case Report ◽

Rare Case ◽

Histopathological Examination ◽

Hair Follicles ◽

Review Of Literature ◽

Solitary Lesion ◽

Biological Potential ◽

Rare Case Report ◽

The Face ◽

Head Neck

ABSTRACT The trichoepithelioma is a benign cutaneous neoplasm which is derived from hair follicles. It is common in the face, but there are only three reports of the solitary occurrence on the nose. It is often not recognized because of its rarity, controversial classification, origin and biological potential. The objective of this paper is to present a case of solitary trichoepithelioma on the nose, histopathological examination and treatment. It should be considered as a differential diagnosis of a solitary lesion of nose which is confused with basal cell carcinoma. The confirmation by histopathological examination is essential. How to cite this article Sah BP, Shilpakar SL, Aryal B, Chettri ST, Pokharel A, Mishra S, Paudel D. Solitary Trichoepithelioma of Nose: A Rare Case Report and Review of Literature. Int J Head Neck Surg 2015;6(3):115-117.

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Eczema herpeticum in an infant – a case report

Pediatria i Medycyna Rodzinna ◽

10.15557/pimr.2020.0059 ◽

2020 ◽

Vol 16 (3) ◽

pp. 320-324

Author(s):

Lesya Besh ◽

◽

Oksana Matsyura ◽

Olesya Besh ◽

Olga Troyanovska ◽

...

Keyword(s):

Atopic Dermatitis ◽

Case Report ◽

Clinical Case ◽

Allergic Inflammation ◽

The Body ◽

Preventive Effect ◽

Herpesvirus Infection ◽

Eczema Herpeticum ◽

The Face ◽

Ulcerative Lesions

Eczema herpeticum is a chronic dermatosis with erosive and ulcerative lesions of the skin in children of a predominantly young age. The clinical case presented in this article shows the severe course of herpesvirus infection combined with atopic dermatitis in a 5-month infant. A rash in the form of vesicles and pustules throughout the body with a predominant localisation on the skin of the face, the scalp, neck, and chest was found in the course of the examination of the child. Influence of infections on the course of allergic processes is an ambiguous and complicated issue. It has been proved that an infection can contribute to the development of allergies and exacerbate the course of already existing allergic inflammation. In recent years, an increasing number of studies have shown the preventive effect of infection on the development of allergic pathology in children, especially during the first years of life.

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Maxillary Carcinosarcoma: A Case Report and Review of the Literature

Otorhinolaryngology Clinics - An International Journal ◽

10.5005/jp-journals-10003-1170 ◽

2014 ◽

Vol 6 (3) ◽

pp. 114-117

Author(s):

Ilson Sepúlveda ◽

Michael Frelinghuysen ◽

Cesar García ◽

M Loreto Spencer ◽

Enrique Platín ◽

...

Keyword(s):

Radiation Therapy ◽

Case Report ◽

Review Of The Literature ◽

The Face ◽

Maxillary Region ◽

Radical Dissection

ABSTRACT We report on a patient who presented with pain and swelling to the left maxillary region of the face. A biopsy of the area was performed and subsequently diagnosed as maxillary carcinosarcoma (CCS). After reviewing the pathology results and the size of the tumor, it was decided that a radical dissection, followed by radiation therapy was the best option. How to cite this article Sepúlveda I, Frelinghuysen M, García C, Spencer ML, Platín E, Alarcon J, Ulloa D. Maxillary Carcinosarcoma: A Case Report and Review of the Literature. Int J Otorhinolaryngol Clin 2014;6(3):114117.

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