scholarly journals Progeroid Syndrome with Mitral Regurgitation: A Rare Case Report

2020 ◽  
Vol 5 (02) ◽  
pp. 117-122
Author(s):  
D. P. Kalyana Chakravarthi ◽  
Yalampati Rama Kishore ◽  
M. Naveen Kumar

AbstractProgeroid syndromes (PS) involve the disorder of early aging. Although survival of progeria syndrome patients is nearly 15 years as per literature, the adult onset progeroid starts manifesting in the third decade. Here, we are presenting a rare case of progeroid at the age of 45 years with mitral regurgitation (MR). The patient has alopecia, dry skin, frontal bossing, up staring eyes with bilateral corneal opacities, prominent nose with parrot beak appearance, thin upper lip, large, low-set ears, periorbital hyperpigmentation, micrognathia, retrognathia, and hyperpigmentation over lower abdomen/both feet and hands. Facial and skeletal manifestation are the major clinical features of the PS; along with the characteristics mentioned above, the patient also had severe eccentric MR. This patient has PS with mitral valve prolapse and severe MR. Most of the features of progeria exist in this patient, which manifested at a younger age. However, the progression of the external features and survival up to 45 years favors PS instead of progeria. Therefore, genetic analysis is mandatory to confirm. We are reporting this case due to the rarity of onset of symptoms within a younger age group; however, the progression of the disease was very slow, which may be a another variant of progeria/PS.

2016 ◽  
Vol 7 (2) ◽  
pp. 210-212
Author(s):  
Kalegowda Deepadarshan ◽  
Bugude Gangadhar ◽  
Mallaiah Mallikarjun

2021 ◽  
Vol 57 (3) ◽  
pp. 256
Author(s):  
Muhammad Husni Tamrin ◽  
Wahjoe Djatisoesanto

Chondrosarcoma is a rare variant of bladder tumor and one of the rare types of soft tissue sarcoma. This case happened on a 36-year-old male who complained of lumps in his lower abdomen, accompanied by difficulties in passing urine and painful urination, without hematuria. We performed TURBT and histopathological examination showed low-grade chondrosarcoma. The patient was diagnosed with low-grade bladder chondrosarcoma. The patient was treated for chemotherapy and radiotherapy. However, after undergoing one cycle of chemotherapy, the patient refused to continue the therapy.


2014 ◽  
Vol 5 (4) ◽  
pp. 478 ◽  
Author(s):  
Subhash Kashyap ◽  
Vinay Shanker ◽  
Neeraj Sharma

2014 ◽  
Vol 04 (04) ◽  
pp. 156-159
Author(s):  
Jayanth Koneru ◽  
Matthew Cholankeril ◽  
Priyank Shah ◽  
Fayez Shamoon ◽  
Hartaj Virk ◽  
...  

2021 ◽  
pp. 142-143
Author(s):  
Navdeep Kaur ◽  
Reeta Dhar ◽  
Arpita Singh ◽  
Vishakha Malhotra

Lipodystrophies are dermatological complications due to repetitive subcutaneous injections leading to subsequent loss of adipose tissue at the site of injection. Fat necrosis occursdue to concentrated pressure on microlobules of adipocytes causing disruption of septa between these microlobules, leading to permanent changes in the injured site. In this report we present a case of 63 year old female who developed lipodystrophy following subcutaneous injection in left lower abdomen.


2021 ◽  
Vol 24 (1) ◽  
pp. E009-E013
Author(s):  
DIR Choudhury ◽  
Saikat DasGupta ◽  
Mauin Uddin ◽  
Siddhartha Shankar Howlader ◽  
PK Chanda ◽  
...  

Ellis-Van Creveld (EVC) syndrome is an autosomal recessive disorder. Around 150 cases are described in published literature and in Bangladesh, it is even rare.  The patient usually comes with short stature, dental deformity, and cardiac deformity. Here, we present the case of a patient with ostium primum atrial septal defect (ASD) with moderate mitral regurgitation who underwent surgical repair of ASD and mitral valve replacement.


Author(s):  
Radhika Batra ◽  
Richa Gautam ◽  
Alpana Manchanda ◽  
Deepak Ghuliani

AbstractGossypiboma is a rare condition caused by retention of a foreign body, most commonly surgical sponge following any surgical procedure. The patient may be asymptomatic, can present with vague symptoms, or rarely with acute symptoms depending on the location of the foreign body and the complications associated with it; thus it may be difficult to diagnose this condition. A 30-year-old woman presented to our hospital with complaints of lump and mild pain on both sides of the lower abdomen for 3 months following caesarean section which was performed in a rural hospital. Ultrasound and computed tomography findings along with the classical history helped in arriving at the diagnosis of two gossypibomas in lower abdomen, one in each flank which was further confirmed on laparotomy.


2014 ◽  
Author(s):  
Tadeusz Budlewski ◽  
Dorota Szydlarska ◽  
Norbert Szalus ◽  
Jolanta Kijek ◽  
Beata Ewa Chrapko

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