Rare Case Report Of Mesenteric Fibromatosis

AbstractMesenteric fibromatosis is a part of the clinical-pathologic spectrum of deep fibromatoses. We report this rare case of primary mesenteric tumor that was diagnosed to be a mesenteric fibromatosis on histopathological examination.In majority of patients it may remain asymptomatic and the management of these tumors depends on histopathological examination. Postoperatively, patient was well and subsequent follow up showed normal recovery.

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Plasma Cell Mucositis - Rare Case Report

Journal of Dentistry and Oral Sciences ◽

10.37191/mapsci-2582-3736-2(3)-043 ◽

2020 ◽

Author(s):

Shailesh Naresh Kokal

Keyword(s):

Case Report ◽

Plasma Cell ◽

Rare Case ◽

Steroid Injection ◽

Histopathological Examination ◽

Incisional Biopsy ◽

Mucosal Surfaces ◽

Patient Reported ◽

Rare Case Report

Plasma cell mucositis (PCM) is a rare benign proliferative disorder affecting various mucosal surfaces usually seen in elderly patients. In the present case, a 66-year-old male patient reported with the complaint of bleeding from the oral cavity and enlarged gums in relation to lower right 1st& 2nd molars. Incisional biopsy of the involved mucosal area confirmed the diagnosis of plasma cell mucositis (PCM). Diagnosis of this condition is complex often needs a biopsy, histopathological examination and immunohistochemistry. Management includes conventional gingivectomy and intra lesional steroid injection. Regular follow up of plasma cell mucositis (PCM) is essential due to the possibility of its clinical persistence. There is the potential involvement of other mucosal surfaces and chances of malignant transformation.

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Traumatic avulsion management by allotransplantation. A rare case report with two years of successful follow-up

International Journal of Medical and Dental Case Reports ◽

10.15713/ins.ijmdcr.22 ◽

2015 ◽

Vol 2 ◽

pp. 1-4

Author(s):

Nandini R. Katta ◽

P. Poornima ◽

A. Shruthi ◽

N. B. Nagaveni

Keyword(s):

Case Report ◽

Rare Case ◽

Rare Case Report

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Mixed Cutaneous Infection Caused byMycobacterium szulgaiandMycobacterium intermediumin a Healthy Adult Female: A Rare Case Report

Case Reports in Dermatological Medicine ◽

10.1155/2015/607519 ◽

2015 ◽

Vol 2015 ◽

pp. 1-4 ◽

Cited By ~ 3

Author(s):

Amresh Kumar Singh ◽

Rungmei S. K. Marak ◽

Anand Kumar Maurya ◽

Manaswini Das ◽

Vijaya Lakshmi Nag ◽

...

Keyword(s):

Case Report ◽

Rare Case ◽

Healthy Adult ◽

Nontuberculous Mycobacteria ◽

Anterior Abdominal Wall ◽

Cutaneous Infection ◽

Once Daily ◽

The Past ◽

Rare Case Report

Nontuberculous mycobacteria (NTMs) are ubiquitous and are being increasingly reported as human opportunistic infection. Cutaneous infection caused by mixed NTM is extremely rare. We encountered the case of a 46-year-old female, who presented with multiple discharging sinuses over the lower anterior abdominal wall (over a previous appendectomy scar) for the past 2 years. Microscopy and culture of the pus discharge were done to isolate and identify the etiological agent. Finally, GenoType Mycobacterium CM/AS assay proved it to be a mixed infection caused byMycobacterium szulgaiandM. intermedium. The patient was advised a combination of rifampicin 600 mg once daily, ethambutol 600 mg once daily, and clarithromycin 500 mg twice daily to be taken along with periodic follow-up based upon clinical response as well as microbiological response. We emphasize that infections by NTM must be considered in the etiology of nonhealing wounds or sinuses, especially at postsurgical sites.

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CHOREA GRAVIDARUM: A RARE CASE REPORT

10.36106/ijsr/7229729 ◽

2021 ◽

pp. 71-72

Author(s):

Aswini Viswanadh ◽

Sujata Singh ◽

Vinnisa N. V

Keyword(s):

Case Report ◽

Family History ◽

Gestational Age ◽

Postpartum Period ◽

Rare Case ◽

Third Trimester ◽

Detailed Evaluation ◽

Rare Case Report

Chorea gravidarum is the term given to chorea occurring during pregnancy. Here, we report a case of 24 year old primigravida at gestational age 38 weeks 3days ,without any signicant past & family history who presented with chorea gravidarum for the rst time in third trimester. On detailed evaluation no etiology was identied. On follow up in postpartum period, her choreiform movements have reduced in intensity, but is still persisting pointing towards an idiopathic origin.

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Solitary Trichoepithelioma of Nose: A Rare Case Report and Review of Literature

International Journal of Head and Neck Surgery ◽

10.5005/jp-journals-10001-1237 ◽

2015 ◽

Vol 6 (3) ◽

pp. 115-117

Author(s):

Sachin Lal Shilpakar ◽

Bivek Aryal ◽

Shyam Thapa Chettri ◽

Apar Pokharel ◽

Deepak Paudel

Keyword(s):

Case Report ◽

Rare Case ◽

Histopathological Examination ◽

Hair Follicles ◽

Review Of Literature ◽

Solitary Lesion ◽

Biological Potential ◽

Rare Case Report ◽

The Face ◽

Head Neck

ABSTRACT The trichoepithelioma is a benign cutaneous neoplasm which is derived from hair follicles. It is common in the face, but there are only three reports of the solitary occurrence on the nose. It is often not recognized because of its rarity, controversial classification, origin and biological potential. The objective of this paper is to present a case of solitary trichoepithelioma on the nose, histopathological examination and treatment. It should be considered as a differential diagnosis of a solitary lesion of nose which is confused with basal cell carcinoma. The confirmation by histopathological examination is essential. How to cite this article Sah BP, Shilpakar SL, Aryal B, Chettri ST, Pokharel A, Mishra S, Paudel D. Solitary Trichoepithelioma of Nose: A Rare Case Report and Review of Literature. Int J Head Neck Surg 2015;6(3):115-117.

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Juvenile Aggressive Trabecular Ossifying Fibroma of Mandible: A Rare Case Report

Journal of Contemporary Dentistry ◽

10.5005/jp-journals-10031-1140 ◽

2016 ◽

Vol 6 (1) ◽

pp. 45-51

Author(s):

Deepa Das Achath ◽

Abhishek Sanjay Ghule ◽

Preeti Kanchan-Talreja ◽

Sunanda Bhatnagar

Keyword(s):

Case Report ◽

Rare Case ◽

Histological Analysis ◽

High Recurrence Rate ◽

Ossifying Fibroma ◽

Appropriate Treatment ◽

Juvenile Ossifying Fibroma ◽

Rare Case Report

ABSTRACT Fibroosseous lesions of the jaws, including juvenile ossifying fibroma (JOF), pose diagnostic and therapeutic difficulties due to their clinical, radiological, and histological variability. There are two histological varieties of it, one as psammomatoid type and second as trebacular type; here, we present a trebacular type, which is a rare variety. After the clinical examination, radiological and histological analysis, it was diagnosed as juvenile trebacular ossifying fibroma. Although JOF is an uncommon clinical entity, its aggressive local behavior and high recurrence rate means that it is important to make an early diagnosis, apply the appropriate treatment, and, especially, follow-up the patient over the long term. How to cite this article Ghule AS, Achath DD, Kanchan- Talreja P, Bhatnagar S. Juvenile Aggressive Trabecular Ossifying Fibroma of Mandible: A Rare Case Report. J Contemp Dent 2016;6(1):45-51.

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Teratoma of larynx: case report

International Journal of Otorhinolaryngology and Head and Neck Surgery ◽

10.18203/issn.2454-5929.ijohns20213909 ◽

2021 ◽

Vol 7 (10) ◽

pp. 1700

Author(s):

Rakesh Srivastava ◽

Vini Tandon

Keyword(s):

Carbon Dioxide ◽

Case Report ◽

Germ Cells ◽

Carbon Dioxide Laser ◽

Rare Case ◽

Histopathological Examination ◽

Flexible Laryngoscopy ◽

First Case ◽

Congenital Teratoma

<p class="abstract">Teratomas are embryonal neoplasm arises from totipotent germ cells. They are having tissues from all the three blastodermic layers. There are various locations of congenital teratoma. Naso-oropharyngeal site teratoma are either sessile or pedunculated. We describe a rare case of laryngeal teratoma in a five years old patient presented with change in voice and breathing difficulty. On flexible laryngoscopy, it appeared like supraglottic cyst but on CT scan it was confirmed as teratoma. Pre-operative tracheostomy and transoral carbon dioxide laser assisted excision done. Histopathological examination showed osteoid trabeculae, chondroid tissue with loose myxoid islands and adipose tissue. No recurrence of tumor on 18 months follow-up. This is the first case report of pediatric larynx teratoma reported in present century.</p>

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Cerebral Coenurosis Masquerading as Malignancy: A Rare Case Report from India

Journal of Neurosciences in Rural Practice ◽

10.4103/jnrp.jnrp_296_18 ◽

2019 ◽

Vol 10 (02) ◽

pp. 367-370

Author(s):

Shamila Mohamed Ali ◽

P. Somashekara Reddy ◽

S. Venugopal ◽

Manmeet Chhabra ◽

Anita Mahadevan

Keyword(s):

Case Report ◽

Characteristic Feature ◽

Rare Case ◽

Histopathological Examination ◽

Surgical Excision ◽

Hydatid Cysts ◽

The Third ◽

Rare Case Report ◽

Cerebral Coenurosis ◽

Cuticular Layer

ABSTRACTHuman coenurosis is a rare zoonotic disease caused by the larvae of Tinea multiceps seen in sheep-rearing countries. We report the case of a 63-year-old male who was referred to our hospital with a working diagnosis of skull base chondrosarcoma. Histopathological examination after surgical excision revealed characteristic feature of coenurus with multiple scolices invaginating from the outer cuticular layer. Coenuri are often mistaken for giant cysticercal cysts and hydatid cysts. Despite its wide prevalence in cattle, only two cases of human coenurosis are reported from India till date. We report the third case from India.

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Human Dirofilariasis Due to D.Repens Presenting as a Chest Wall Swelling : A Rare Case Report

Journal of Health and Allied Sciences NU ◽

10.1055/s-0040-1703559 ◽

2012 ◽

Vol 02 (01) ◽

pp. 51-53

Author(s):

Harish S. Permi ◽

Pretty D'Souza ◽

K.R. Bhagavan ◽

Mary Raju ◽

Pooja Sarda

Keyword(s):

Chest Wall ◽

Rare Case ◽

Histopathological Examination ◽

Chest Wall Tumor ◽

Anopheles Mosquitoes ◽

Chest Wall Tumors ◽

Rare Case Report ◽

Human Dirofilariasis ◽

Wall Tumor

AbstractPrimary Dirofilariasis is caused by a Zoonotic filarial nematode. It is transmitted to humans by Culex, Aedes, or Anopheles mosquitoes, which ingest blood-containing microfilaria from affected dogs, cats, or raccoons. Chest wall tumors are uncommon lesions that originate from blood vessels, nerves, bone, cartilage, or fat. We report a case of Human Dirofilariasis due to D. Repens occurring in the chest wall in a 32 year old male. Clinical diagnosis of benign chest wall tumor was considered and it was excised. Histopathological examination confirmed it as Dirofilaria repens. On regular follow up he is doing fine.

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