scholarly journals Sporotrichosis of Maxillary Sinus

2011 ◽  
Vol 2 (3) ◽  
pp. 269-271 ◽  
Author(s):  
NC Sandeepa ◽  
HP Jaishankar ◽  
B Sharath Chandra ◽  
SN Veena ◽  
T Yeshaswini
Keyword(s):  
Maxillary Sinus ◽  
Rare Case ◽  
Antifungal Agents ◽  
Immunocompetent Patient ◽  
The Body ◽  
Causative Organism ◽  
Fungal Culture ◽  
Mode Of Entry ◽  
Mycotic Disease ◽  
Deep Fungal Infection

ABSTRACT Sporotrichosis or Gardener's disease is a chronic nodular subcutaneous mycotic disease, causative organism being Sporotrichum schenckii. The specific mode of entry of the fungus into the body, being mainly through small cuts and punctures and rarely by inhalation; which usually manifest as cutaneous and subcutaneous infections. Here we report a rare case of sporotrichosis of maxillary sinus in an immunocompetent patient. Our case of sporotrichosis, a deep fungal infection involving maxillary sinus was confirmed by fungal culture and successfully managed by antifungal agents combined with surgical debridement.

A Rare Case of Tuberculous Prostatitis

2016 ◽  
Vol 1 (2) ◽  
pp. 33
Author(s):  
Nurul Yaqeen Mohd Esa ◽  
Mohammad Hanafiah ◽  
Marymol Koshy ◽  
Hilmi Abdullah ◽  
Ahmad Izuanuddin Ismail ◽  
...  
Keyword(s):  
Rare Case ◽  
Correct Diagnosis ◽  
Immunocompetent Patient ◽  
Clinical Suspicion ◽  
Tuberculosis Infection ◽  
Advanced Age ◽  
Immunocompromised Patients ◽  
Prostatic Biopsy ◽  
High Clinical Suspicion

Tuberculous prostatitis is an uncommon form of tuberculosis infection. It is commonly seen in immunocompromised patients and in those of middle or advanced age. The diagnosis is often not straight forward due to the nature of its presentation. We report a case of tuberculous prostatitis in a young, healthy and immunocompetent patient, who initially presented with respiratory features, followed by episodes of seizures and testicular swelling. He was finally diagnosed with tuberculous prostatitis after prostatic biopsy. This case illustrates that in a high TB prevalence environment, when symptoms warrant, there should be a high clinical suspicion coupled with a thorough approach in order to arrive at a correct diagnosis of TB prostatitis.

Linezolid Induced Skin Reactions in a Multi Drug Resistant Infective Endocarditis Patient: A Rare Case

2020 ◽  
Vol 15 (3) ◽  
pp. 222-226 ◽  
Author(s):  
Asha K. Rajan ◽  
Ananth Kashyap ◽  
Manik Chhabra ◽  
Muhammed Rashid
Keyword(s):  
Case Report ◽  
Infective Endocarditis ◽  
Rare Case ◽  
Case Reports ◽  
Multidrug Resistant ◽  
The Body ◽  
Prior History ◽  
Skin Reactions ◽  
Rare Case Report ◽  
Multiple Drugs

Rationale: Linezolid (LNZ) induced Cutaneous Adverse Drug Reactions (CADRs) have rare atypical presentation. Till date, there are very few published case reports on LNZ induced CADRs among the multidrug-resistant patients suffering from Infective Endocarditis (MDR IE). Here, we present a rare case report of LNZ induced CARs in a MDR IE patient. Case report: A 24-year-old female patient was admitted to the hospital with chief complaints of fever (101°C) associated with rigors, chills, and shortness of breath (grade IV) for the past 4 days. She was diagnosed with MDR IE, having a prior history of rheumatic heart disease. She was prescribed LNZ 600mg IV BD for MDR IE, against Staphylococcus coagulase-negative. The patient experienced flares of cutaneous reactions with multiple hyper-pigmented maculopapular lesions all over the body after one week of LNZ therapy. Upon causality assessment, she was found to be suffering from LNZ induced CADRs. LNZ dose was tapered gradually and discontinued. The patient was prescribed corticosteroids along with other supportive care. Her reactions completely subsided and infection got controlled following 1 month of therapy. Conclusion: Healthcare professionals should be vigilant for rare CADRs, while monitoring the patients on LNZ therapy especially in MDR patients as they are exposed to multiple drugs. Moreover, strengthened spontaneous reporting is required for better quantification.

Rare case of Ureaplasma parvum septic arthritis in an immunocompetent patient

2020 ◽  
Vol 13 (9) ◽  
pp. e236396
Author(s):  
Abuzar Ali Asif ◽  
Moni Roy ◽  
Sharjeel Ahmad
Keyword(s):  
Septic Arthritis ◽  
Rare Case ◽  
Immunocompetent Patient ◽  
Next Generation ◽  
Ureaplasma Parvum ◽  
Urogenital Infections ◽  
Joint Infections ◽  
Prosthetic Joint ◽  
Prosthetic Joint Infections ◽  
Diagnostic Modalities

Mycoplasmatacea family comprises two genera: Mycoplasma and Ureaplasma. Ureaplasma parvum (previously known as U. urealyticum biovar 1) commonly colonises the urogenital tract in humans. Although Ureaplasma species have well-established pathogenicity in urogenital infections, its involvement in septic arthritis has been limited to prosthetic joint infections and immunocompromised individuals. We present a rare case of native right knee infection due to U. parvum identified using next-generation sequencing of microbial cell-free DNA testing and confirmed with PCR assays. This rare case of Ureaplasma septic arthritis was diagnosed using newer next-generation DNA sequencing diagnostic modalities and a literature review of prior cases, antibiotic coverage and antimicrobial resistance is incorporated as part of the discussion.

scholarly journals The Bacteriological Examinations of the Faeces in Four Cases of Typhoid Fever, made at frequent intervals for a period of one month

1924 ◽  
Vol 23 (1) ◽  
pp. 106-116 ◽  
Author(s):  
Leonard P. Lockhart
Keyword(s):  
Typhoid Fever ◽  
Physical State ◽  
Intestinal Flora ◽  
High Carbohydrate Diet ◽  
The Body ◽  
Causative Organism ◽  
Carbohydrate Diet ◽  
High Carbohydrate ◽  
Large Numbers

1. The appearance and disappearance of typhoid bacilli in the faeces in these four cases bore no relation to changes in the diet nor to the physical state of the stools, but the later they appeared the shorter was the duration of their appearance.On the disappearance of typhoid bacilli from the stools the intestinal flora tended to become more simple.2. B. coli was the only organism invariably present at every examination.3. Streptococci were very much more abundant in the earlier stages of the disease, when milk formed the greater part of the diet, than in the later stages.4. In two cases where boils occurred on the body the causative organism had previously been isolated in large numbers from the faeces.5. With stools slightly alkaline to litmus the flora in these cases was relatively simple and fermentative in type. There is no apparent advantage, therefore, in giving a high carbohydrate diet except in cases of marked alkalinity and putrefaction.

scholarly journals Infected Dentigerous Cyst of Maxillary Sinus Arising from an Ectopic Third Molar

2013 ◽  
Vol 3 ◽  
pp. 7 ◽  
Author(s):  
Yadavalli Guruprasad ◽  
Dinesh Singh Chauhan ◽  
Umashankar Kura
Keyword(s):  
Maxillary Sinus ◽  
Rare Case ◽  
Dentigerous Cyst ◽  
Third Molar ◽  
Radiographic Examination ◽  
Palpable Mass ◽  
Follicular Cyst ◽  
Pathologic Features ◽  
Dentigerous Cysts ◽  
Ectopic Third Molar

A dentigerous cyst or follicular cyst is a form of odontogenic cyst. It is believed that it forms during the development of the tooth and is associated with pressure exerted by the crown of an unerupted (or partially erupted) tooth on the fluid within the follicular space. Typically, dentigerous cysts are painless and discovered during routine radiographic examination. However, they may be large and result in a palpable mass. Additionally, as they grow they displace adjacent teeth. They almost exclusively occur in permanent dentition. The cyst is lined by stratified squamous non-keratinizing epithelium. About 70% of dentigerous cysts occur in the mandible and 30% in the maxilla. Dentigerous cysts associated with ectopic teeth within the maxillary sinus are very rare. We report radiologic and pathologic features in a rare case of infected dentigerous cyst of maxillary sinus arising from an ectopic third molar in a 21-year-old female patient.

scholarly journals A Case of Hydatid Cyst of Thyroid Gland

2013 ◽  
Vol 5 (2) ◽  
pp. 143-145 ◽  
Author(s):  
Arpan Kumar Dey ◽  
Pijush Kanti Mandal ◽  
Agnibha Dutta ◽  
Subhraprakash Pramanik ◽  
Saurabh Maji ◽  
...  
Keyword(s):  
Thyroid Gland ◽  
Hydatid Cyst ◽  
Rare Case ◽  
Medical Science ◽  
Science Volume ◽  
The Body ◽  
Multinodular Goitre ◽  
Primary Hydatid Cyst ◽  
The Brain ◽  
Thyroid Lesions

Hydatid cyst may be found in almost any part of the body, but most often in the liver and the lungs. Other organs affected occasionally include the brain, muscle, kidney, heart, pancreas, adrenal, and thyroid gland. Hydatidosis located in the thyroid is an infrequent finding, even in endemic regions. This report documents a rare case with a cystic nodule in the thyroid detected by ultrasonography. The patient was a 30-year-old woman with an euthyroid multinodular goitre. Ultrasonography revealed a cystic nodule, and the ultrasonic appearance of the cyst liquid showed multiple echoes, suggesting that the nodule could be a hydatid cyst. The histopathologic examinations confirmed this to be a primary hydatid cyst of thyroid. During the differential diagnosis of the cystic thyroid lesions, hydatid disease of the thyroid gland should be considered in endemic areas. Chemotherapy is necessary to avoid recurrence. DOI: http://dx.doi.org/10.3126/ajms.v5i2.8830 Asian Journal of Medical Science, Volume-5(2) 2014: 143-145

scholarly journals Talaromikosis Marneffei

2019 ◽  
Vol 12 (2) ◽  
pp. 72
Author(s):  
Sem S. Surja ◽  
Robiatul Adawiyah ◽  
Retno Wahyuningsih
Keyword(s):  
Endemic Area ◽  
Clinical Manifestations ◽  
Its Region ◽  
Clinical Suspicion ◽  
Cross Wall ◽  
Respiratory Disorder ◽  
Fungal Culture ◽  
Talaromyces Marneffei ◽  
Mycotic Disease ◽  
Histopathology Examination

Talaromycosis marneffei is a mycotic disease caused by Talaromyces marneffei which primarily infectimmunocompromised patient. This disease is endemic in Southeast Asia, and Indonesia consider as endemic area dueto a case of tourist who got the infection after visiting Indonesia. Diagnosis was made based on clinical suspicion withlaboratory confirmation. Clinical manifestations are not specific, such as fever, anemia, weight loss, lymphadenopathy,hepatomegaly, splenomegaly, respiratory disorder, and cutaneous manifestation. Histopathology and culture are themost common examination performed for diagnosis. In histopathology examination, fungi appear as fission arthroconidiacells which shape round to oval, with cross wall formation inside or outside macrophage and histiocyte. Thermaldimorphism characteristic can be observed in fungal culture. Fungi grows as mold at 25oC-30oC and as yeast at 37oC.Definitive identification of T. marneffei was done by molecular examination using primers derived from ITS region asprimary marker and beta tubulin region as secondary marker. Talaromyces marneffei is sapronosis, that transmitted viainhalation of conidia from environment.

scholarly journals A RARE CASE OF HEMIPLEGIA

2020 ◽  
pp. 30-30
Author(s):  
Valeti Rajeswari ◽  
Kolluru V D Karthik ◽  
Srinivasula Sriranga Pravallika
Keyword(s):  
Cerebral Infarction ◽  
Honey Bee ◽  
Anaphylactic Shock ◽  
Rare Case ◽  
The Body ◽  
Intravenous Fluids ◽  
Rare Entity ◽  
Bee Sting ◽  
The Face

Honey bee sting induced Cerebral infarction is a rare entity . We report a case of 55year old male presented with anaphylactic shock following honey bee sting along with weakness of left side of the body and the face . He was managed with anti histaminics, adrenaline injections, Intravenous fluids , vasopressors , anti platelets and anticoagulants .

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