A rare case of atrioventricular extrasystole due to myocarditidis produetivae instilaris and congenital functional stenosis of the left venous opening

2021 ◽  
Vol 20 (1) ◽  
pp. 30-36
Author(s):  
V. N. Korovkina ◽  
V. A. Vasilyeva
Keyword(s):  
Rare Case ◽  
Unusual Case

Among the cardiological material of our Clinic, we encountered the following completely unusual case, which we had the opportunity to observe.

A rare case of toxocariasis presenting with hypereosinophilic pericardial effusion and mycotic aneurysm

2021 ◽  
pp. 004947552110343
Author(s):  
Sapna Sandal ◽  
Gopal Krishnan ◽  
Ashish Sharma ◽  
Javed Ismail ◽  
Jaivinder Yadav
Keyword(s):  
Pericardial Effusion ◽  
Rare Case ◽  
Mycotic Aneurysm ◽  
Unusual Case ◽  
Paediatric Population ◽  
Parasitic Infections ◽  
Intermittent Fever ◽  
Tropical Countries

Parasitic infections are the leading cause of hypereosinophilia in the paediatric population in tropical countries. We report an unusual case of Toxocara infection in an eight-year-old boy who presented with intermittent fever, hypereosinophilia complicated by massive pericardial effusion and a mycotic aneurysm. This child received treatment with four weeks of albendazole and steroids.

scholarly journals A rare case of unilateral postaxial duplicated foot in a developmentally normal child

2017 ◽  
Vol 25 (1) ◽  
pp. 230949901668498 ◽  
Author(s):  
Haniza Sahdi ◽  
Chan Wai Hoong ◽  
Ahmad Hata Rasit ◽  
Fredy Arianto ◽  
Lau Kiew Siong ◽  
...  
Keyword(s):  
Popliteal Artery ◽  
Normal Child ◽  
Rare Case ◽  
Unusual Case ◽  
Organ System ◽  
Lateral Aspect ◽  
Posterior Branch ◽  
Rare Congenital Disorder ◽  
Definitive Surgery ◽  
Radiological Studies

Diplopodia, being a rare congenital disorder, is infrequently discussed in published texts. Most reported cases have accounted the involvement of duplicated preaxial digits with other associated organ system and physical deformities. Here, we present an unusual case of isolated diplopodia involving postaxial toes in a child with no other organ and physical abnormalities. Radiological studies revealed a set of 10-digit-duplicated foot over the lateral aspect of the native foot, complete with phalanges and its corresponding metatarsals as well as tarsals, supplied by an anomalous posterior branch of the popliteal artery. Definitive surgery was performed just before the child was learning to walk.

scholarly journals Bilateral Sturge Weber Syndrome- a rare case report

2013 ◽  
Vol 5 (1) ◽  
pp. 129-132 ◽  
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

scholarly journals Isolated hydatid cyst of thyroid: An unusual case

Ultrasound ◽  
2018 ◽  
Vol 26 (4) ◽  
pp. 251-253
Author(s):  
Sonay Aydin ◽  
Cihat Tek ◽  
Fatma Dilek Gokharman ◽  
Erdem Fatihoglu ◽  
Pinar Nercis Kosar
Keyword(s):  
Rare Case ◽  
Unusual Case ◽  
Definitive Diagnosis ◽  
Cystic Disease ◽  
Parasitic Infestation ◽  
Intermediate Hosts ◽  
Laboratory Findings ◽  
Hydatic Cyst ◽  
Antiparasitic Drugs ◽  
Animal Feces

Introduction Hydatid cystic disease is a parasitic infestation that is mostly caused by Echinococcus granulosus, which is common in sheep-rearing areas of the Mediterranean, Middle East, Australia, New Zealand, South Africa, and South America. Canines are the definitive hosts, and herbivores (e.g. sheep, horses, deer) or humans are intermediate hosts. Ingested eggs from animal feces hatch in the gut and release oncospheres (immature forms of the parasite enclosed in an embryonic envelope). Case report A very rare case of isolated, thyroidal, hydatic cyst is presented. Conclusion Non-vascular cysts may be seen on ultrasonographic examination that are not specific for hydatid disease. Clinical and laboratory findings are therefore important. Definitive diagnosis is based on histopathological findings. Treatment is surgical and antiparasitic drugs are required after surgery.

Unusual Case of Sclerosing Angiomatoid Nodular Transformation of the Spleen in an Adolescent Patient: Case Report and Literature Review

2021 ◽  
Vol 6 (1) ◽  
Author(s):  
Abboud B ◽  
◽  
Honein K ◽  
Aidibi A ◽  
Yared F ◽  
...  
Keyword(s):  
Rare Case ◽  
Unusual Case ◽  
Benign Lesion ◽  
Relevant Literature ◽  
Clinical Suspicion ◽  
Radiographic Examination ◽  
Patient Case ◽  
Sclerosing Angiomatoid Nodular Transformation ◽  
High Clinical Suspicion ◽  
Red Pulp

Sclerosing Angiomatoid Nodular Transformation (SANT) is a rare and benign lesion arising from the red pulp of the spleen, with an unknown etiopathogenesis. These tumors are usually asymptomatic and are found incidentally on radiographic examination. Therefore, high clinical suspicion is of great importance for the diagnosis. Splenectomy provides complete cure, and no recurrence and/or malignant transformation was reported to date. In this study, a rare case of SANT was reported in aadolescent male, and was discussed with the relevant literature.

scholarly journals Two New Species of Taygetina With a Possible Case of ‘Juxta Loss’ in Butterflies (Lepidoptera: Nymphalidae: Satyrinae)

2019 ◽  
Vol 3 (6) ◽  
Author(s):  
Shinichi Nakahara ◽  
Pável Matos-Maraví ◽  
Eduardo P Barbosa ◽  
Keith R Willmott ◽  
Gerardo Lamas ◽  
...  
Keyword(s):  
New Species ◽  
Species Diversity ◽  
Molecular Phylogeny ◽  
Rare Case ◽  
Unusual Case ◽  
Single Species ◽  
Character State ◽  
State Change ◽  
Two New Species ◽  
A New Species

Abstract The male genitalic characters of Hexapoda are well known for their great taxonomic and systematic value. Despite insect male genitalia displaying large diversity, variation, and modification across orders, some structures are consistently present, and such characters can serve as the basis for discussion regarding homology. In the order Lepidoptera, a male genitalic structure widely known as the ‘juxta’ is present in many taxa and absence or modification of this character can be phylogenetically informative at the generic or higher level. We here focus on the systematics of the so-called ‘Taygetis clade’ within the nymphalid subtribe Euptychiina, and report an unusual case of ‘juxta loss’ in a single species, Taygetina accacioi Nakahara & Freitas, n. sp., a new species from Brazil named and described herein. Additionally, we describe another west Amazonian Taygetina Forster, 1964 species, namely Taygetina brocki Lamas & Nakahara, n. sp., in order to better document the species diversity of Taygetina. Our most up-to-date comprehensive molecular phylogeny regarding ‘Taygetis clade’ recovered these two species as members of a monophyletic Taygetina, reinforcing the absence of juxta being a character state change occurring in a single lineage, resulting in an apomorphic condition, which we report here as a rare case in butterflies (Papilionoidea).

scholarly journals Intersphincteric epidermoid inclusion cyst: report of a rare case

2020 ◽  
Vol 2020 (3) ◽  
Author(s):  
James Ashcroft ◽  
Betania Mahler-Araujo ◽  
Richard J Davies
Keyword(s):  
Case Report ◽  
Surgical Technique ◽  
Rare Case ◽  
Unusual Case ◽  
Accurate Diagnosis ◽  
Rare Entity ◽  
Inclusion Cyst ◽  
Patient Morbidity ◽  
Perineal Region ◽  
Epidermoid Inclusion Cyst

Abstract Epidermoid inclusion cysts of the perineal region are a rare entity, which require appropriate diagnosis and management. Here we describe the unusual case of a large protruding epidermoid inclusion cyst originating from the intersphincteric anal plane, which was mobilized and excised successfully. Essential investigations to ensure accurate diagnosis in addition to surgical technique to reduce recurrence and patient morbidity are described in this case report.

A rare case of nasal gout

2020 ◽  
Vol 13 (10) ◽  
pp. e234788
Author(s):  
Emma Richards ◽  
Emma Watts ◽  
Lisha McClelland
Keyword(s):  
Disease Progression ◽  
Metabolic Disorder ◽  
Rare Case ◽  
Unusual Case ◽  
Metatarsophalangeal Joint ◽  
First Metatarsophalangeal Joint ◽  
Nasal Bones ◽  
Acute Attacks ◽  
Work Up ◽  
Nose And Throat

Gout is an increasingly common metabolic disorder worldwide. Classical presentation is with acute attacks of arthritis affecting the first metatarsophalangeal joint. With disease progression, tophi may also appear. We present an unusual case of nasal gout in a 55-year-old man who was referred to the Ear, Nose and Throat department with irregularity over the nasal bones and episodic pain. We discuss the work up, diagnosis and management of this case and review the limited literature on this topic.

ENTRAPMENT OF THE MEDIAN NERVE BETWEEN SUBLIMIS TENDONS AFTER DISTAL FOREARM FRACTURE: AN UNUSUAL CASE REPORT

Hand Surgery ◽  
2008 ◽  
Vol 13 (02) ◽  
pp. 111-114
Author(s):  
Y. Taniguchi ◽  
T. Kitano ◽  
T. Shimoe ◽  
M. Yoshida
Keyword(s):  
Case Report ◽  
Median Nerve ◽  
Rare Case ◽  
Nerve Palsy ◽  
Unusual Case ◽  
Forearm Fracture ◽  
Distal Forearm ◽  
Distal Forearm Fracture ◽  
Median Nerve Palsy ◽  
Unusual Case Report

We present a rare case of entrapment of the median nerve between sublimis tendons after fractures of the distal radius and ulna in an 80-year-old woman. The entrapped median nerve was elongated redundantly with two regions of constriction. To our knowledge, no case of median nerve palsy caused by such a factor has been previously reported.

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