Abstract #1063: An Unusual Case of Recurrent Postpartum Thyroiditis in a Male Patient

2015 ◽  
Vol 21 ◽  
pp. 223
Author(s):  
Regina Belokovskaya ◽  
Alice Levine
2021 ◽  
pp. 13-14
Author(s):  
VPS Punia ◽  
Apoorva Shetty ◽  
Prashant Prashant ◽  
Akash Bharti ◽  
Praveen Raman Mishra ◽  
...  

Psoriasis is known to cause chronic inammatory disorder of the skin through an immune mediated mechanism, it may be complicated by different types of glomerular lesions. Three different mechanisms have been implicated by which psoriasis can cause renal damage: immune-mediated renal damage, drug-related renal damage and chronic renal damage. This report presents a case of 35 years old male patient with extensive psoriasis, who presented to our hospital with nephrotic syndrome


2018 ◽  
Vol 56 (1) ◽  
pp. 110-115 ◽  
Author(s):  
Sapna Radia ◽  
Alexander C. Cash ◽  
Kanwalraj Moar

We describe an unusual case of an odontogenic keratocyst (OKC) associated with an ungrafted left-sided alveolar cleft in a 10-year-old male patient. There is no previous report in the literature of OKC or other dental cysts associated with an alveolar cleft. We discuss the management of the OKC prior to secondary bone grafting and present this case to highlight the difficulty in the management of OKC concurrent with grafting of the alveolar cleft site, the proximity of unerupted permanent teeth, and possible treatment modalities.


2012 ◽  
Vol 2012 ◽  
pp. 1-2 ◽  
Author(s):  
A. Aber ◽  
A. Tahir ◽  
V. Arumuham ◽  
G. Smith ◽  
S. Almpanis

Benign cystic mesothelioma of the tunica vaginalis is a rare occurrence. It usually presents with painless gradual swelling in the scrotum. These types of benign mesotheliomas typically occur in the peritoneum and usually affect young to middle-aged patients. We present in this case an unusual case of benign cystic mesothelioma of the tunica vaginalis in a 77-year-old male patient.


2012 ◽  
Vol 2012 ◽  
pp. 1-3 ◽  
Author(s):  
Monica Yadav ◽  
Sugandha Ghonasgi ◽  
Rohit Shah ◽  
S. M. Meghana

Familial progressive hyperpigmentation (FPH) is a rare genodermatosis characterized by hyperpigmented patches in the skin and mucous membranes, present in early infancy, and increase in size and number with age. The genetic basis for FPH remains unknown. We report an unusual case of familial progressive hypermelanosis in a 17-year-old male patient with family history, who presented with a peculiar progressive oral pigmentation disorder. Diagnosis was confirmed by a series of hematological, biochemical, and histopathological investigations. Our paper stresses the need for the dentist to be aware of the systemic conditions that can also manifest in the oral cavity.


2015 ◽  
Vol 49 (3) ◽  
pp. 143-145
Author(s):  
Jotideb Mukhopadhyay ◽  
Manoj Kumar Roy ◽  
Apratim Chatterjee ◽  
Anup Sarkar ◽  
Koushik Roy ◽  
...  

ABSTRACT In 1963, Liddle et al described a disorder that looks like the features of primary aldosteronism, characterized by severe hypertension and hypokalemia but with negligible secretion of aldosterone. They theorized that this was ‘a disorder in which the renal tubles transport ions with such facility that the end result simulates that of a mineralocorticoid excess’. Liddle's syndrome involves abnormal kidney function, with excess reabsorption of sodium and loss of potassium from the renal tubule, and is treated with a combination of low sodium diet and potassiumsparing diuretic drugs (e.g. amiloride). We are reporting a case of 48 years known hypertensive patient admitted with acute onset quadriparesis, ultimately diagnosed as hypokalemia due to Liddle's syndrome, treated with low sodium salt and potassium sparing diuretics-amiloride responds dramatically. How to cite this article Roy MK, Chatterjee A, Sarkar A, Roy K, Lahiri D, Agarwal R, Mukhopadhyay S, Mukhopadhyay J. An Interesting Unusual Case of Hypokalemic Quadriparesis in 48 Years Hypertensive Male Patient: A Liddle's Syndrome. J Postgrad Med Edu Res 2015;49(3):143-145.


2017 ◽  
Vol 2017 ◽  
pp. 1-3 ◽  
Author(s):  
Dinghai Luo ◽  
Liping Ye ◽  
Weidan Wu ◽  
Haihong Zheng ◽  
Xinli Mao

We present an unusual case of a 41-year-old male patient with a large lymphangioma of the esophagus. Endoscopy revealed that the structure measured 60 × 10 mm in the mucosa and the submucosa and had a heterogenous echo pattern. The esophageal mass was successfully resected by endoscopic piecemeal mucosal resection. However, most esophageal lymphangiomas that are larger than 2 cm in diameter reported in the literature can be removed only through open surgery. Thus far, we know of no reported cases of endoscopic resection as a treatment for this case.


2015 ◽  
Vol 357 ◽  
pp. e436-e437
Author(s):  
F.J. Nakasone ◽  
A.S. Bossoni ◽  
F. Freua ◽  
S.E. Senaha ◽  
D.A. Gripp ◽  
...  

2017 ◽  
Vol 2017 ◽  
pp. 1-6
Author(s):  
Nidhi Manaktala ◽  
Karen Boaz ◽  
Krupa Mehta Soni ◽  
Srikant Natarajan ◽  
Junaid Ahmed ◽  
...  

Verrucous proliferation arising from odontogenic cysts is a rare entity. We report an unusual case of an infected odontogenic cyst with verrucous proliferation and melanin pigmentation in a 13-year-old male patient who presented with an intraoral swelling in relation to impacted teeth 26 and 27. The enucleated lesion was diagnosed as an odontogenic keratocyst and the patient died within two years of presentation due to multiple recurrences. The clinical, radiological, and microscopic features of the lesion are presented with an attempt to discuss the etiopathogenesis. The case hereby reported is uncommon with only eight cases reported in the literature.


2017 ◽  
Vol 2017 ◽  
pp. 1-4 ◽  
Author(s):  
Joana Ruivo Rodrigues ◽  
Gonçalo Roque Santos

Arachnoid granulations are structures filled with cerebrospinal fluid (CSF) that extend into the venous sinuses through openings in the dura mater and allow the drainage of CSF from subarachnoid space into venous system. Usually they are asymptomatic but can be symptomatic when large enough to cause sinus occlusion. We report a rare case of a brain herniation into a giant arachnoid granulation in an asymptomatic elderly male patient, which was discovered incidentally.


1991 ◽  
Vol 5 (5) ◽  
pp. 179-183 ◽  
Author(s):  
Franzjosef Schweiger ◽  
Jasim Radhi

Both primary biliary cirrhosis and celiac disease may be asymptomatic in many patients for extended periods of time. Rarely the disorders have been reported to occur together, in which case symptomatic malabsorption and diarrhea are virtually always present. An unusual case is presented of an asymptomatic male patient who had both primary biliary cirrhosis and celiac disease. The literature describing this coexistence, and theories regarding a common etiological link between the two disorders, are reviewed.


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