Inflammatory myofibroblastic tumor of hard palate: a lesion of extreme rarity

Pandya, Naman Kirit; Bhatt, Utsav

doi:10.11604/pamj.2021.38.267.28236

Cited by 17 publications

(16 citation statements)

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“…Only age-specific techniques, categorisation criteria, and treatment objectives may be used to conduct meaningful laboratory and clinical research. (20)(21)(22)(23)(24)(25)(26)(27)(28)(29)(30)(31)(32)(33)…”

Section: Discussionmentioning

confidence: 99%

Childhood Systemic Lupus Erythematosus; A Rare Multisystem Life-threatening Disorder: a case of 13 years-old-girl with oral involvement and joint pain as primary clinical manifestation

2022

pnr

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Systemic lupus erythematosus (SLE) is an autoimmune illness that affects several organs, and the most frequent renal consequence of SLE is lupus nephritis (LN). It is a rare, systemic disease, possibly fatal autoimmune illness with high morbidity. SLE prevalence has been observed to range between 14 and 60 per 100,000 people. A 13-year-female child was admitted to the hospital in the paediatric ward with the chief complaint of skin lesion over sun sun-exposed and bleeding from oral mucosa. Blood samples were sent to the laboratory for investigations, and blood cultures were also sent to the microbiology lab. As soon as she was admitted, treatment was started without any delay. Blood investigations show a decreased level of WBC count, i.e. 3500 cu/mm, and the blood culture revealed the organism's growth. Hence patient was started on injectable antibiotics. After 15 days of a continuous course of antibiotics, the patient started recovery. The rashes started disappearing a little bit. Physiotherapy is begun for a child with joint pain where she experiences relief.

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Section: Discussionmentioning

confidence: 99%

Childhood Systemic Lupus Erythematosus; A Rare Multisystem Life-threatening Disorder: a case of 13 years-old-girl with oral involvement and joint pain as primary clinical manifestation

2022

pnr

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“…The majority of surgeons consider turricephaly surgical avoidance to be preferable to therapy and turribrachycephaly correction to be difficult, possibly dangerous, and visually unsatisfactory. (10)(11)(12)(13)(14)(15)(16)(17)(18)(19)(20)(21)Treatment options for turricephaly in one stage have been discussed. According to a procedure revealed in a study by Persing et al turricephaly can be cured with just one surgery.…”

Section: Discussion:-mentioning

confidence: 99%

Case Report on Turricephaly

dhale¹,

Taksande²,

Bhagat³

2022

Journal of Pharmaceutical Negative Results

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Turricephaly is regarded as one of the most challenging cranial malformations to treat because increasing intracranial pressure can occur when cranial height is reduced. In typical medical and nursing situations, kids with turricephaly can be identified by thier osteogenesis imperfecta, ophthalmic proptosis, hydrocephalus, and certain facial characteristics such substantial temporal steamrolling, facial asymmetry hypoplasia, and micrognathia.Turricephaly is a rare and potentially fatal autoimmune disease. In the beginning, estimates of turricephaly from antiquity to the present are shown, and in the end, the findings of a personal investigation into the generally disturbed social behaviour and A 4 year male child admited in pediatric department in hospital the patient reported Head swelling, nausea, occipital area swelling, both eyes swelling, and irregular skull form. the primary therapeutic interventions was given to the patient and he was treated with syp zincovit 5 ml BD antibiotic intravenous fluids during hospitalization and the treatment was continued until my final day of care.

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“…You may be limited in your activities depending on the extent and severity of the disease. To prevent future infection, your healthcare professional may recommend that you take treatment for a long time [12,13,14].…”

Section: Discussionmentioning

confidence: 99%

A Rare Case of Anaplastic Astrocytoma

Durgam

Ghungrud

Alwadkar

et al. 2021

JPRI

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Introduction: In adult’s glioblastoma is the most common malignant tumor, which occurs due to the abnormal growth of astrocytes cells. Slightly it is more common in men than females. Standard and quality of care and advanced treatment make a positive impact on patients’ quality of life. However, glioblastoma cannot be cured completely, but treatment approaches such as radiation and chemotherapy may improve the clinical course, but these treatments often takes a heavy toll. Case Presentation: Here we are reporting about a 45 -years-old male who is admitted to Acharya Vinoba Bhave Rural Hospital. With the complaints of headache, for 1 year, history of seizure 2 episodes 3 months before then patient is on antiepileptic medication. Patient was conscious with altered mental status. By radiological investigation, it was revealed that there was a right occipital region glioma tradition necrosis was present. In his family, there was no history of hypertension, diabetes mellitus. On physical examination, s1 and s2 sounds were present and it was normal. The tumor was invading the parenchyma of the right transverse sinus. Dura opened in a cruciate manner, the tumor decompress internally which was vascular, and suck able tumor base interface found. Then patient underwent malignant glioma excision i.e., gross total resection of the tumor was done under general anesthesia. After that, he managed with antibiotics, analgesics, antiepileptic, and anti-edema, now the patient was neurologically stable and he was shifted toward. His histopathology report shows anaplastic astrocytoma. Now patient was in stable condition. Hence being discharged with follow-up after 15 days in Neuro OPD. Conclusion: Glioma is a brain tumor that affects the human body. There is a poor prognosis of this disease and survival time, therapy is limited. But early diagnosis and treatment patients can spend quality of life.

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Inflammatory myofibroblastic tumor of hard palate: a lesion of extreme rarity

Cited by 17 publications

References 0 publications

Childhood Systemic Lupus Erythematosus; A Rare Multisystem Life-threatening Disorder: a case of 13 years-old-girl with oral involvement and joint pain as primary clinical manifestation

Childhood Systemic Lupus Erythematosus; A Rare Multisystem Life-threatening Disorder: a case of 13 years-old-girl with oral involvement and joint pain as primary clinical manifestation

Case Report on Turricephaly

A Rare Case of Anaplastic Astrocytoma

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