Urolithiasis in a female miniature potbellied pig

2019 ◽  
Vol 7 (3) ◽  
pp. e000809
Author(s):  
Abigail Needleman ◽  
Ricardo Videla
Keyword(s):  
Case Report ◽  
Calcium Phosphate ◽  
Physical Examination ◽  
Blood Count ◽  
Complete Blood Count ◽  
Female Adult ◽  
Abdominal Radiographs ◽  
History Of ◽  
Management Changes ◽  
Phosphate Carbonate

A five-year-old female spayed Vietnamese potbellied pig was evaluated due to a chronic history of dysuria and pollakiuria as well as lack of faecal output for one week. Physical examination revealed vitals within normal parameters and to facilitate further workup evaluation, the patient was anaesthetized. Complete blood count and chemistry panel values were unremarkable. Ultrasonography of the bladder indicated the presence of uroliths, and this was confirmed with abdominal radiographs. A cystotomy was performed to remove the uroliths, and an enaema was administered to relieve the constipation. The patient recovered from anaesthesia uneventfully and was discharged after four days of hospitalisation. Analysis revealed that the stones were composed of calcium phosphate carbonate; husbandry and medical management changes were implemented to prevent reoccurrence. Urolithiasis is an uncommon finding in female pigs; this case report describes a comprehensive clinical workup and treatment of a female adult pig with urolithiasis.

scholarly journals Case Report: A rare cause of vaginal bleeding at Keren Zonal Referral Hospital, Eritrea

F1000Research ◽  
2021 ◽  
Vol 8 ◽  
pp. 37
Author(s):  
Million Abraha ◽  
Shiden Solomon
Keyword(s):  
Case Report ◽  
Diagnostic Tests ◽  
Vaginal Bleeding ◽  
Blood Count ◽  
Complete Blood Count ◽  
Referral Hospital ◽  
Regional Referral Hospital ◽  
Holy Water ◽  
History Of

Vaginal bleeding due to leech infestation is a very uncommon but important gynaecological problem. This report presents the case of a 65-year-old woman who presented to Keren Regional Referral Hospital, Eritrea, with vaginal bleeding of two and half weeks duration, dizziness and fatigue. On the day of her admission complete blood count and speculum exam were done and she was diagnosed with anaemia due to cervical leech infestation. Routine speculum exam for vaginal bleeding is recommended in cases with history of holy water or springs visits to prevent unnecessary diagnostic tests and for rapid management.

scholarly journals Isolated Submental Lymphadenopathy

2021 ◽  
Vol 2 (5) ◽  
pp. 01-03
Author(s):  
Lynnette J Mazur ◽  
Micah Gibson ◽  
Vikas Gupta ◽  
Hunter Nolen
Keyword(s):  
Physical Examination ◽  
Medical History ◽  
Blood Count ◽  
Complete Blood Count ◽  
Past Medical History ◽  
Perioral Dermatitis ◽  
History Of

A 5 year old female presented to clinic with a lump under her chin. She had a similar lump two months ago but the parents stated that it spontaneously resolved in a few days. There was no history of fever and there were no pets. Her past medical history was significant for epilepsy which was controlled with zonisamide. On physical examination a 3x2.5 cm, soft, nontender, nonmobile submental mass and perioral dermatitis were noted. (Figures 1, 2) A complete blood count (CBC) and an ultrasound (US) were ordered.

BILATERAL PROPTOSIS - INITIAL AND RARE PRESENTATION: AML

2021 ◽  
pp. 17-18
Author(s):  
Tejasvini Chandra ◽  
Perwez Khan ◽  
Lubna Khan ◽  
Anshika Gupta
Keyword(s):  
Myeloid Leukemia ◽  
Blood Count ◽  
Complete Blood Count ◽  
Rare Condition ◽  
Metastatic Tumour ◽  
Blood Picture ◽  
Rare Presentation ◽  
Radiological Investigation ◽  
Presumptive Diagnosis ◽  
History Of

We report bilateral proptosis as the initial presentation of Acute Myeloid Leukemia (AML) in a child. An Eight year child presented with a history of painless proptosis in the both eyes within 10 days. Radiological investigation (CT scan) showed inltration of orbit with the metastatic tumour cell. AML was diagnosed with complete blood count, General Blood Picture (GBP) and bone marrow biopsy. The presumptive diagnosis of leukemic inltration of the orbit is made. We report this case as AML can rarely present in child as a bilateral proptosis due to leukemic inltration. Urgent treatment modality for this rare condition is radiation.

scholarly journals Graham-Little Piccardi Lassueur Syndrome: case report

2012 ◽  
Vol 87 (5) ◽  
pp. 775-777 ◽  
Author(s):  
Raquel Bissacotti Steglich ◽  
Renata Elise Tonoli ◽  
Giselle Martins Pinto ◽  
Fernanda Melo Müller ◽  
Isabelle Maffei Guarenti ◽  
...  
Keyword(s):  
Case Report ◽  
Physical Examination ◽  
Hair Follicles ◽  
Rare Disorder ◽  
Rare Syndrome ◽  
Scarring Alopecia ◽  
History Of

A 33-year-old woman presented with a 3-year history of progressive alopecia of the scalp. Past treatment with hydroxicloroquine did not show improvement. Physical examination revealed multiple areas of alopecia with atrophic aspect of the scalp, and axillary and pubic hypotrichosis. Dermoscopy showed hyperkeratosis and accentuation of follicular ostia. Anatomopathological examination revealed decrease in the number of hair follicles, upper perifollicular infiltrate and areas with fibrosis. The Piccardi-Lassueur-Graham-Little syndrome is a rare disorder, characterized by the triad of multifocal scarring alopecia of the scalp, keratotic follicular eruption and hypotrichosis of axillary and pubic regions. Management is a challenge and many medications tried have controversial results. We report a case of this rare syndrome which improved with corticoids.

scholarly journals Extensive nasopharyngeal angiofibroma – case report

1970 ◽  
Vol 15 (2) ◽  
pp. 75-77
Author(s):  
M Alamgir Chowdhury ◽  
Mousumi Malakar ◽  
SM Golam Rabbani ◽  
Naseem Yasmeen ◽  
Shahidul Islam
Keyword(s):  
Case Report ◽  
Physical Examination ◽  
Nasal Cavity ◽  
Neck Region ◽  
Lateral Rhinotomy ◽  
Male Population ◽  
Vascular Neoplasm ◽  
Nasopharyngeal Angiofibroma ◽  
Recurrent Epistaxis ◽  
History Of

Juvenile nasopharyngeal angiofibroma is a benign vascular neoplasm, but it is locally aggressive. This accounts for less than 0.5% of all the neoplasm in the head & neck region in the male population only. Here we report a case of 10-year-old boy with a blackish red smooth polypoidal mass in the nasal cavity, with history of recurrent epistaxis. On physical examination it was suspected as nasopharyngeal angiofibroma. We removed it totally by lateral rhinotomy approach. And the diagnosis was nasopharyngeal angiofibroma on histopathology. Key words: Angiofibroma; Nasopharyngeal. DOI: 10.3329/bjo.v15i2.5061 Bangladesh J Otorhinolaryngol 2009; 15(2): 75-77

scholarly journals UNILATERAL SPECTACULOTOMY ON A BURMESE PYTHON (Python bivittatus) WITH SUBSPECTACULAR ABSCESS: A CASE REPORT

2020 ◽  
Author(s):  
Puveanthan Nagappan Govendan ◽  
Lynn Kaat Laura Kurniawan
Keyword(s):  
Case Report ◽  
Oral Cavity ◽  
Physical Examination ◽  
Respiratory Infection ◽  
Chief Complaint ◽  
Intravenous Catheter ◽  
Topical Antibiotic ◽  
Female Adult ◽  
Python Bivittatus ◽  
The Right

A three year old female adult albino Python bivittatus weighing 12 kilograms was presented with a chief complaint of right spectacle growth and whitening. The snake also had a respiratory infection which started about 2 weeks prior to being presented. Physical examination showed bubbly nostrils, inflammation on the right eye, inflammation on the right palatum of the oral cavity, and crackling sound during auscultation when exhaling and hissing. The snake was diagnosed with subspectacular abscess and respiratory infection. Spectaculotomy was performed under general and local anesthesia. All abscesses were removed using a sterile sexing probe while continuously flushing the eye. Topical antiseptic was diluted and flushed into the eye before topical antibiotic eye ointment was applied. Post-operative treatment included daily flushing using an intravenous catheter, eye ointment application, and administration of systemic antibiotic and NSAID to treat the co-related respiratory infection. Three weeks after the surgery the snake went through ecdysis, after which the snake regained its appetite and recovery was thereafter significantly improved.

scholarly journals Compound Presentation: A Case Report of One of the Rarest Varieties- Vertex, Hand, and Feet Presentation

2021 ◽  
Vol 8 (2) ◽  
Author(s):  
Sium AF ◽  
◽  
Tilahun A ◽  
Mersha A ◽  
Yihun S ◽  
...  
Keyword(s):  
Case Report ◽  
Physical Examination ◽  
Cesarean Delivery ◽  
Conservative Management ◽  
Similar Type ◽  
Cervical Dilation ◽  
Compound A ◽  
Case Summary ◽  
Spontaneous Correction ◽  
History Of

Background: Compound presentation occurs in approximately 1/700 deliveries. Being the rarest type, there is scarce literature about the recommended management for vertex-hand-feet variety of compound presentation. We report a similar type of compound presentation. Case Summary: A 25 years-old primigravida who claimed to be 9 months ammenorric presented with a history of pushing down pain of 12 hours duration with associated history of passage of liquor of 4 hours duration. Up on physical examination she was in active first of labor at cervical dilation of 5 centimeters and the presentation was compound- a vertex-hand-feet variety. Cesarean delivery was done after two hours of conservative management and the outcome was an alive 2300grams male neonates with no perinatal or maternal complication. Conclusion: In the rarest variety of compound presentation, which is a vertex, hand, and feet type, spontaneous correction is unusual if the fetus is alive and interference is usually necessary.

scholarly journals First Autochthonous Infection of a Cat with Dirofilaria immitis in Austria

Pathogens ◽  
2021 ◽  
Vol 10 (9) ◽  
pp. 1104 ◽  
Author(s):  
Lisa-Maria Kulmer ◽  
Maria Sophia Unterköfler ◽  
Hans-Peter Fuehrer ◽  
Varvara Janovska ◽  
Matus Pagac ◽  
...  
Keyword(s):  
Case Report ◽  
Dirofilaria Immitis ◽  
Complete Blood Count ◽  
Clinical Signs ◽  
Surgical Removal ◽  
Negative Results ◽  
Heartworm Disease ◽  
History Of ◽  
One Year ◽  
The Right

This case report is about a seven-year-old male neutered European Shorthair cat infected by Dirofilaria immitis as the first reported autochthonous Dirofilaria immitis infection in Austria. There was no history of periods abroad. Echocardiography showed suspected D. immitis in the right cardiac chamber with increased pulmonary pressure and ascites. Surgical removal of the heartworms was performed. Twenty adult heartworms were removed by transvenous jugular approach under general anesthesia and stored in 4% formalin. Five out of 20 specimens were examined via light and stereomicroscopy and feline heartworm infection was confirmed. Amplification of a 203 bp or 724 bp fragment of the cytochrome c oxidase subunit I gene was unsuccessful. After surgery the cat developed acute renal failure but recovered quickly. One year later, the cat underwent a control examination including echocardiography and blood work. There were no more D. immitis detectable at echocardiography. Lung pressure was mildly increased. Complete blood count and creatinine were unremarkable. The Knott’s test and Dirofilaria-Antigen-test produced negative results. The cat did not show any clinical signs during the follow-up period. The aim of this case report is to highlight the growing risk of acquiring infection with D. immitis not only for Austrian dogs, but also for cats. This case report represents the first report of autochthonous D. immitis infection in Austria. Moreover, even if the prognosis in cats with caval syndrome due to feline heartworm disease is guarded to poor, surgical removal of the filariae can be a successful treatment option.

scholarly journals Idiopathic Hypertrophic Pachymeningitis: A Case Report from Bangladesh

2018 ◽  
Vol 3 (2) ◽  
pp. 110-112
Author(s):  
Meera Momtaz Sabeka ◽  
Md Nazrul Islam
Keyword(s):  
Case Report ◽  
Physical Examination ◽  
Optic Atrophy ◽  
Severe Headache ◽  
Imaging Studies ◽  
Hypertrophic Pachymeningitis ◽  
History Of ◽  
Diagnostic Clue ◽  
Work Up ◽  
Rule Out

A 52 years old lady presented with sudden severe headache with the history of similar intense headache twenty years back which ended up with left sided blindness. Her physical examination was unremarkable except optic atrophy of the left eye. Investigation included biochemical work up, imaging studies and CSF study. The MRI of brain with contrast gave the key diagnostic clue with characteristic findings of hypertrophic pachymeningitis. Other investigations helped to rule out possible etiologies and the diagnosis idiopathic hypertrophic pachymeningitis was finally made. The patient has been treated with steroid and enjoyed improvement in her yearlong symptoms.Journal of National Institute of Neurosciences Bangladesh, 2017;3(2): 110-112

scholarly journals   PCR for detection of tick-borne Anaplasma phagocytophilum pathogens: a review

2011 ◽  
Vol 56 (No. 11) ◽  
pp. 577-580 ◽  
Author(s):  
Z. Adamiak ◽  
A. Pomianowski ◽  
M. Kwiatkowska ◽  
A. Majchrowski ◽  
H. Matyjasik ◽  
...  
Keyword(s):  
Case Report ◽  
Surgical Technique ◽  
Anaplasma Phagocytophilum ◽  
Blood Count ◽  
Complete Blood Count ◽  
Abdominal Cavity ◽  
Peritoneal Catheter ◽  
Shunt Implantation ◽  
English Bulldog ◽  
Ventriculo Peritoneal Shunt

This article describes the procedure of ventriculo-peritoneal shunt implantation in an English bulldog with laparoscopy-assisted placement of the peritoneal catheter in the abdominal cavity. Prior to surgery, the patient was subjected to physical and neurological examinations involving a complete blood count (CBC), biochemistry profiling, EEG and MRI. This case report also describes the patient’s pharmacological treatment before the procedure, the applied surgical technique and the benefits of the laparoscopy-assisted approach.  

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