Skip Navigation Links.
Collapse <span class="m110 colortj mt20 fontw700">Volume 12 (2024)</span>Volume 12 (2024)
Issue 3, Volume 12, 2024
Issue 2, Volume 12, 2024
Issue 1, Volume 12, 2024
Collapse <span class="m110 colortj mt20 fontw700">Volume 11 (2023)</span>Volume 11 (2023)
Issue 12, Volume 11, 2023
Issue 11, Volume 11, 2023
Issue 10, Volume 11, 2023
Issue 9, Volume 11, 2023
Issue 8, Volume 11, 2023
Issue 7, Volume 11, 2023
Issue 6, Volume 11, 2023
Issue 5, Volume 11, 2023
Issue 4, Volume 11, 2023
Issue 3, Volume 11, 2023
Issue 2, Volume 11, 2023
Issue 1, Volume 11, 2023
Collapse <span class="m110 colortj mt20 fontw700">Volume 10 (2022)</span>Volume 10 (2022)
Issue 12, Volume 10, 2022
Issue 11, Volume 10, 2022
Issue 10, Volume 10, 2022
Issue 9, Volume 10, 2022
Issue 8, Volume 10, 2022
Issue 7, Volume 10, 2022
Issue 6, Volume 10, 2022
Issue 5, Volume 10, 2022
Issue 4, Volume 10, 2022
Issue 3, Volume 10, 2022
Issue 2, Volume 10, 2022
Issue 1, Volume 10, 2022
Collapse <span class="m110 colortj mt20 fontw700">Volume 9 (2021)</span>Volume 9 (2021)
Issue 12, Volume 9, 2021
Issue 11, Volume 9, 2021
Issue 10, Volume 9, 2021
Issue 9, Volume 9, 2021
Issue 8, Volume 9, 2021
Issue 7, Volume 9, 2021
Issue 6, Volume 9, 2021
Issue 5, Volume 9, 2021
Issue 4, Volume 9, 2021
Issue 3, Volume 9, 2021
Issue 2, Volume 9, 2021
Issue 1, Volume 9, 2021
Collapse <span class="m110 colortj mt20 fontw700">Volume 8 (2020)</span>Volume 8 (2020)
Issue 12, Volume 8, 2020
Issue 11, Volume 8, 2020
Issue 10, Volume 8, 2020
Issue 9, Volume 8, 2020
Issue 8, Volume 8, 2020
Issue 7, Volume 8, 2020
Issue 6, Volume 8, 2020
Issue 5, Volume 8, 2020
Issue 4, Volume 8, 2020
Issue 3, Volume 8, 2020
Issue 2, Volume 8, 2020
Issue 1, Volume 8, 2020
Collapse <span class="m110 colortj mt20 fontw700">Volume 7 (2019)</span>Volume 7 (2019)
Issue 12, Volume 7, 2019
Issue 11, Volume 7, 2019
Issue 10, Volume 7, 2019
Issue 9, Volume 7, 2019
Issue 8, Volume 7, 2019
Issue 7, Volume 7, 2019
Issue 6, Volume 7, 2019
Issue 5, Volume 7, 2019
Issue 4, Volume 7, 2019
Issue 3, Volume 7, 2019
Issue 2, Volume 7, 2019
Issue 1, Volume 7, 2019
Collapse <span class="m110 colortj mt20 fontw700">Volume 6 (2018)</span>Volume 6 (2018)
Issue 12, Volume 6, 2018
Issue 11, Volume 6, 2018
Issue 10, Volume 6, 2018
Issue 9, Volume 6, 2018
Issue 8, Volume 6, 2018
Issue 7, Volume 6, 2018
Issue 6, Volume 6, 2018
Issue 5, Volume 6, 2018
Issue 4, Volume 6, 2018
Issue 3, Volume 6, 2018
Issue 2, Volume 6, 2018
Issue 1, Volume 6, 2018
Collapse <span class="m110 colortj mt20 fontw700">Volume 5 (2017)</span>Volume 5 (2017)
Issue 12, Volume 5, 2017
Issue 11, Volume 5, 2017
Issue 10, Volume 5, 2017
Issue 9, Volume 5, 2017
Issue 8, Volume 5, 2017
Issue 7, Volume 5, 2017
Issue 6, Volume 5, 2017
Issue 5, Volume 5, 2017
Issue 4, Volume 5, 2017
Issue 3, Volume 5, 2017
Issue 2, Volume 5, 2017
Issue 1, Volume 5, 2017
Collapse <span class="m110 colortj mt20 fontw700">Volume 4 (2016)</span>Volume 4 (2016)
Issue 12, Volume 4, 2016
Issue 11, Volume 4, 2016
Issue 10, Volume 4, 2016
Issue 9, Volume 4, 2016
Issue 8, Volume 4, 2016
Issue 7, Volume 4, 2016
Issue 6, Volume 4, 2016
Issue 5, Volume 4, 2016
Issue 4, Volume 4, 2016
Issue 3, Volume 4, 2016
Issue 2, Volume 4, 2016
Issue 1, Volume 4, 2016
Collapse <span class="m110 colortj mt20 fontw700">Volume 3 (2015)</span>Volume 3 (2015)
Issue 12, Volume 3, 2015
Issue 11, Volume 3, 2015
Issue 10, Volume 3, 2015
Issue 9, Volume 3, 2015
Issue 8, Volume 3, 2015
Issue 7, Volume 3, 2015
Issue 6, Volume 3, 2015
Issue 5, Volume 3, 2015
Issue 4, Volume 3, 2015
Issue 3, Volume 3, 2015
Issue 2, Volume 3, 2015
Issue 1, Volume 3, 2015
Collapse <span class="m110 colortj mt20 fontw700">Volume 2 (2014)</span>Volume 2 (2014)
Issue 12, Volume 2, 2014
Issue 11, Volume 2, 2014
Issue 10, Volume 2, 2014
Issue 9, Volume 2, 2014
Issue 8, Volume 2, 2014
Issue 7, Volume 2, 2014
Issue 6, Volume 2, 2014
Issue 5, Volume 2, 2014
Issue 4, Volume 2, 2014
Issue 3, Volume 2, 2014
Issue 2, Volume 2, 2014
Issue 1, Volume 2, 2014
Collapse <span class="m110 colortj mt20 fontw700">Volume 1 (2013)</span>Volume 1 (2013)
Issue 1, Volume 1, 2013

Volume 4, Issue 2

Reactive Solitary Eccrine Syringofibroadenoma: A Very Rare Adnexal Tumour of Skin
Case Report
Eccrine syringofibroadenoma (ESFA) is a very rare benign tumour of intraepidermal part (acrosyringium) of eccrine sweat duct. Based on the evidence of known aetiological factors, two forms have been proposed: reactive ESFA and non-reactive ESFA. Rarely, non-reactive forms have been seen to be associated with ectodermal dysplasia. Reactive type has been considered as hyperplastic or hamartomatous response to many inflammatory and neoplastic dermatoses. Owing to its clinical similarity with other chronic dermatoses like deep mycoses, squamous cell carcinoma, diabetic foot ulcer or leprous neuropathic ulcer, it may remain misdiagnosed. Distinctive histopathological features with or without immunostaining usually confirm the diagnosis. ESFA is a very rare entity as to the best of my knowledge, only around 50 cases have been reported all over the world till date. Herein we report a case of reactive solitary ESFA on the right foot in a 65 years old male.
prescription transfer coupon copay cards for prescription drugs free coupon for viagra
coupons for viagra click drug discount coupons
discount prescription coupons link discount prescription drug card
internet drug coupons floridafriendlyplants.com viagra prescription coupon
how many women cheat storyofcheating.com why do people cheat
the cost of an abortion health risks of abortion how long does an abortion take
avodart buy uk go avodart buy uk
American Journal of Medical Case Reports. 2016, 4(2), 71-73. DOI: 10.12691/ajmcr-4-2-10
Pub. Date: March 23, 2016
14098 Views2953 Downloads3 Likes
Cyclic Cushing Syndrome, an Enigma in Diagnosis- A Case Report
Case Report
Cyclic Cushing syndrome is a rare disorder, characterized by repeated episodes of cortisol excess interspersed by periods of normal cortisol secretion. We report a 15-year-old boy with clinical Cushing syndrome and intermittent central Adrenocorticotropic hormone(ACTH) hypersecretion for a period of 8 years. Periods of hypercotisolemia as evidenced clinically and/or biochemically alternated with periods of eucortisolemia leading to much diagnostic dilemma. Ultimately, we were able to demonstrate the episodes of three peaks and two troughs of cortisol secretion favoring our diagnosis. His initial sellar MRI was negative, later high resolution dynamic sellar MRI unmasked a Pituitary micro-adenoma. In the absence of consensus for trans-sphenoidal adenomectomy (TSA) medical management in the form of sodium valproate was prescribed. At present he is on regular follow-up with marked clinical improvement.
discount prescription drug cards open cialis prescription coupon
late termination of pregnancy abortion clinics in los angeles how early can you get an abortion
can i take naproxen with prednisone canitake.net can i take naproxen with prednisone
can i take antabuse and naltrexone can i take antabuse and naltrexone can i take antabuse and naltrexone
prescription transfer coupon click free prescription drug cards
abortion pro life legal abortion abortion clinics in birmingham al
pro abortion after abortion care how to get a abortion
low blood sugar blood sugar control
niacin centauricom.com niasinamid
avodart buy uk go avodart buy uk
American Journal of Medical Case Reports. 2016, 4(2), 65-70. DOI: 10.12691/ajmcr-4-2-9
Pub. Date: March 11, 2016
21081 Views4092 Downloads3 Likes
A Rare Cause of Bilateral Facial Palsy
Case Report
HIV infection can cause neurological complications at all stages of the disease. Bilateral facial paralysis is not common in HIV, and more likely to have a systemic cause such as GBS, brain stem encephalitis, sarcoidosis, Lyme disease, syphilis or bacterial meningitis. Although HIV-associated bilateral facial palsy is very rare, it should be included in the differential diagnosis in unexplained cases, particularly in high-risk patients. We report a unique case of bilateral facial nerve palsy as an initial presenting symptom of AIDS, with an updated literature review.
valacyclovir 1g blog.dotnetnerd.dk levofloxacin
at home abortions areta.se how late can you have an abortion
bystolic discount coupon bystolic savings card program bystolic coupon 2014
bystolic generic name what is the generic for bystolic
free prescription discount cards codesamples.in drug coupons
selegilin preis bhvormegeter.site selegilin tabletta
American Journal of Medical Case Reports. 2016, 4(2), 62-64. DOI: 10.12691/ajmcr-4-2-8
Pub. Date: March 02, 2016
7355 Views3126 Downloads
Gastric Sarcoidosis: A Difficult to Diagnose Rare Disease
Case Report
Gastrointestinal sarcoidosis is a rare clinical entity. Diagnosis of isolated gastric sarcoidosis is difficult as it is usually asymptomatic; when symptomatic it presents with non-specific symptoms such as abdominal pain, nausea and vomiting. We here present a case of a 32-year-old black lady who presented with non-specific abdominal complaints; a diagnosis gastric sarcoidosis was established following endoscopic biopsy. Here symptoms resolved promptly with steroidal therapy as with most cases. Gastric sarcoidosis should be suspected in sarcoid patients who present with nonspecific abdominal complaints. This case serves as an important clinical reminder of the atypical manifestations of sarcoidosis.
women cheat on men how to cheat on husband married men who cheat
copay cards for prescription drugs cialis coupons from lilly printable coupons for cialis
azithromycin pill site viagra 130mg
valacyclovir 1g blog.dotnetnerd.dk levofloxacin
viagra coupons printable paine.edu prescriptions coupons
late termination of pregnancy http://abortionpill-online.com/ how early can you get an abortion
cialis gel blog.devparam.com cialis forum hr
imodium rapid imodium rapid imodium valerie
American Journal of Medical Case Reports. 2016, 4(2), 58-61. DOI: 10.12691/ajmcr-4-2-7
Pub. Date: March 01, 2016
20311 Views4063 Downloads1 Likes
Six-Vessel Spontaneous Coronary Artery Dissection and Vertebral Artery Dissection in Fibromuscular Dysplasia
Case Report
Fibromuscular dysplasia is a non-inflammatory and non-atherosclerotic arteriopathy commonly affecting medium-size renal, carotid, and vertebral arteries. Involvement of the coronary artery is very rare but may cause life-threatening spontaneous dissection. Because it is rare, this disease may go unrecognized. A unique angiographic finding of non-coronary arteries can make an early diagnosis, and prompt treatment is paramount. In this paper, we report on a multiple vessel coronary artery dissection in a female patient who presented with acute stroke symptoms secondary to spontaneous dissection of the left vertebral artery. To date, this is the first case report of the spontaneous dissection of six branches of coronary arteries and the vertebral artery due to fibromuscular dysplasia.
zovirax prednisolone 5mg levofloxacin 500mg
neurontin 400mg site zovirax pill
discount drug coupons viagra coupons from pfizer viagra coupon card
how many women cheat my boyfriend cheated on me quotes why do people cheat
abortion debate fyter.cn what is the abortion pill
pro abortion when can you have an abortion how to get a abortion
bystolic discount coupon bystolic savings card bystolic coupon 2014
amoxicillin bivirkninger link amoxicillin rash
selegilin preis bhvormegeter.site selegilin tabletta
American Journal of Medical Case Reports. 2016, 4(2), 55-57. DOI: 10.12691/ajmcr-4-2-6
Pub. Date: March 01, 2016
11378 Views5047 Downloads1 Likes
Primary Signet-ring Cell Carcinoma of the Uterine Corpus: A Case Report and Review of the Literature
Case Report
Pure signet-ring cell carcinomas of the uterine corpus usually raise the suspicion for a metastatic tumor from other primary sites, e.g., breast or the gastrointestinal tract. And if primary in the uterus, it is more commonly of uterine cervical origin with secondary involvement of the corpus. In general, pure mucinous carcinoma of the endometrium is rare and pure signet-ring cell carcinoma, a form of mucinous carcinoma, is even rarer. Only sparse case reports of primary mucinous adenocarcinoma of the uterine corpus with signet-ring cell features have been described in literature. We report here a case of pure mucinous signet-ring cell carcinoma of the uterine corpus in a 63 year-old morbidly obese woman.
levofloxacin 250mg site prednisolone 10mg
zithromax pill diprolene 0.05% tadalafil
cipro 250mg shouldersofgiants.co.uk sildenafil citrate 200mg
naltrexone serdarnas.com diprolene 0.05%
coupons for viagra click drug discount coupons
discount prescription drug cards read cialis prescription coupon
at home abortions areta.se how late can you have an abortion
prescription transfer coupon site free prescription drug cards
linzess patient assistance linzess patient assistance generic bystolic
cialis dosage levels cialis dosage for a 65 year old man cialis dosing guidelines
low blood sugar blood sugar control
American Journal of Medical Case Reports. 2016, 4(2), 51-54. DOI: 10.12691/ajmcr-4-2-5
Pub. Date: February 27, 2016
11931 Views3324 Downloads
Ascending Sensory Neuropathy caused by Mild Thiamine Deficiency after Gastric Bypass Surgery
Case Report
Bariatric surgery is the current modality of choice for weight loss in morbid obese patients. Although bariatric surgery is well known to improve obesity related complications, however, patients may be affected by early and late complications. Nutritional deficiency is one of the late complications of bariatric surgery which is more common in patients who are non compliant with dietary recommendations. American Society for Metabolic & Bariatric Surgery stresses the importance of long term regular follow up for dietary adherence assessment and nutritional deficiency screening tests. Thiamine deficiency, though rare, is increasingly seen due to increasing population of patients with gastric bypass surgery. Thiamine deficiency after bariatric surgery usually presents with neurological symptoms, most commonly as Wernicke Encephalopathy or dry Beriberi, and in almost all such cases, thiamine deficiency is very severe. Isolated ascending sensory neuropathy is a very rare presentation, which was seen in out patients with mildly low thiamine levels.
can i take antabuse and naltrexone can i take antabuse and naltrexone can i take antabuse and naltrexone
online viagra cheap viagra problems side effects viagra problems side effects
cialis discount coupons sporturfintl.com 2015 cialis coupon
avodart buy uk avodart hair loss avodart buy uk
amoxicillin bivirkninger choice-cottages.co.uk amoxicillin rash
American Journal of Medical Case Reports. 2016, 4(2), 48-50. DOI: 10.12691/ajmcr-4-2-4
Pub. Date: February 25, 2016
13781 Views4769 Downloads2 Likes
Type 1 Cryoglobulinemia in Monoclonal Gammopathy Presenting as Acute Renal Failure and Fatal Outcome
Case Report
The cryoglobulinemia , particularly type 1 or monoclonal, is a rare disease with variable severity and diverse clinical manifestations and may lead to death due to multisystem failure and secondary infections. The early recognition and treatment of this disease are essential for a good prognosis. We report a case of cryoglobulinemic disease associated with Monoclonal gammopathy of Undetermined Significance with fatal outcome.
discount prescription coupons read discount prescription drug card
how many women cheat storyofcheating.com why do people cheat
pet prescription discount card open lilly cialis coupon
tudorza patient assistance go bystolic generic
bystolic generic name what is the generic for bystolic
generic cialis lipseysguns.com www.cialis.com coupon
coupons for prescription drugs link drug coupons
cialis coupons free eblogin.com cialis discount coupons online
cipromed click ciprol
antepsin til hest antepsin alternative antepsin endikasyon
selegilin preis selegilin beipackzettel selegilin tabletta
American Journal of Medical Case Reports. 2016, 4(2), 44-47. DOI: 10.12691/ajmcr-4-2-3
Pub. Date: February 24, 2016
12001 Views3815 Downloads3 Likes
An Unusual Site of Metastasis of Malignant Mixed Müllerian Tumor of the Uterus
Case Report
Malignant mixed Müllerian tumors (carcinosarcomas) are biphasic tumors of the uterus and uterine cervix with carcinomatous and sarcomatous components. Malignant mixed Müllerian tumors (MMMT) are rare tumors, accounting for <5% of uterine cancers. They most commonly metastasize to the vagina, pelvic wall, lungs, and ovaries. We report a unique case of MMMT, which developed in a 69-year-old woman after she presented with hip and knee pain. Ultimately, her pain was found to be caused by metastatic tumor deposits in her psoas muscle. The primary tumor was found to be a MMMT of the uterine corpus. We recommend practitioners be aware of this entity and include it and other metastatic lesions in their differential diagnosis in difficult cases of non-resolving pain.
women love to cheat meet and cheat why wife cheat
zithromax pill click tadalafil
viagra discounts coupons allied.edu coupons for viagra
info on abortion read average abortion cost
cialis savings and coupons blog.nvcoin.com new prescription coupons
cialis gel blog.devparam.com cialis forum hr
American Journal of Medical Case Reports. 2016, 4(2), 41-43. DOI: 10.12691/ajmcr-4-2-2
Pub. Date: February 23, 2016
12987 Views4188 Downloads
Stress Cardiomyopathy: A Case of Apical Ballooning Syndrome followed by Mid-ventricular Ballooning Syndrome as Recurrence
Case Report
Stress cardiomyopathy has an association with emotional or physical stressors and is found to be more common in postmenopausal women. It has a similar presentation as acute myocardial infarction. Involvement of apex at the initial presentation and recurrence at the mid ventricular segment is rare. We describe a case of a 46 year old female with apical involvement at the initial presentation but mid ventricular involvement at the recurrence. 46 year old woman developed sharp chest pain while giving awards at an honors assembly. She was brought to the ER and was found to have a troponin level elevation without any EKG changes. Cardiac cath did not show coronary artery disease. ECHO revealed a low EF of 30 % with apical ballooning. Patient's symptoms resolved and her EF normalized on repeat ECHO. 2 years later patient developed similar symptoms. She had a troponin elevation without EKG changes. ECHO revealed mid-ventricular ballooning with a low EF. Patient's symptoms again resolved and repeat ECHO showed a normalized EF. Our patient had two different episodes of stress cardiomyopathy. Recurrence rate has been reported up to 11.4 percent in previous studies (5). This case is unique as recurrence was at different anatomic locations i.e apex followed by the mid ventricular segments. Further research is needed to understand the underlying mechanisms associated with the stress cardiomyopathy as current hypothesis do not completely explain the disease.
discount prescriptions online cogimator.net free coupon sites
coupons for prescription drugs free prescription cards cialis coupon free
drug coupon card go prescription discount coupon
bystolic generic name what is the generic for bystolic
acheter viagra en ligne avec acheter viagra en ligne avec acheter viagra en ligne avec
reglan bez recepta site reglan upute
escitalopram afbouwen click escitalopram teva
American Journal of Medical Case Reports. 2016, 4(2), 38-40. DOI: 10.12691/ajmcr-4-2-1
Pub. Date: February 22, 2016
10950 Views2811 Downloads5 Likes