Displaying all 12 publications

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  1. Subha ST, Prepageran N
    Med J Malaysia, 2005 Mar;60(1):103-5.
    PMID: 16250292
    Inverted papilloma is the most common benign tumor of nose and paranasal sinuses arising from lateral nasal wall and middle meatus. Histologically these tumors are composed of epithelial nests that are inverted, exophytic and cylindrical. Here we describe a clinical case of nasal cylindrical cell papilloma, which was treated by endoscopic excision.
    Matched MeSH terms: Nose Neoplasms/diagnosis*
  2. Chiun KC, Tang IP, Tharumalingam V, Nurshaline Pauline HK
    Med J Malaysia, 2012 Feb;67(1):131-2.
    PMID: 22582569 MyJurnal
    To report an unusual location of infrasellar craniopharyngioma in a peadiatric patient.
    Matched MeSH terms: Nose Neoplasms/diagnosis*
  3. Prepageran N, Gopala K, Subramaniam KN
    Med J Malaysia, 2002 Dec;57(4):493-5.
    PMID: 12733177
    We describe two cases of nasal inverted papilloma who had different management modalities. Although both were essentially of the same pathology, one underwent endoscopic excision while the other was treated with the more popular lateral rhinotomy and medial maxillectomy. We wish to highlight the different modalities of treatment available for inverted papilloma and a review of published results.
    Matched MeSH terms: Nose Neoplasms/diagnosis
  4. Amin JM, Merican S, Nazarina AR
    Med J Malaysia, 1992 Jun;47(2):147-9.
    PMID: 1494335
    Malignant lymphoma of nasal septum is uncommon. It presents a problem in diagnosis to both otorhinolaryngologist and pathologist. This case report is about one such patient in whom the local disease has been controlled with the treatment of radiotherapy alone. However it is suggested that combined treatment of radiotherapy and cytotoxic therapy might improve the survival rate.
    Matched MeSH terms: Nose Neoplasms/diagnosis
  5. V S, Thamby SP, Al-Hatamleh MAI, Mohamud R, Abdullah B
    Gulf J Oncolog, 2019 Sep;1(31):83-89.
    PMID: 31591996
    BACKGROUND: Natural Killer/T-cell non-Hodgkin lymphomas are rare and aggressive disease of non-Hodgkin lymphoma characterized by angioinvasion, angiodestruction and necrosis. It has a strong association with Epstein-Barr virus (EBV) as the lymphoma cells are almost invariably infected with the clonal episomal form of EBV. Because of their rarity, it is a challenge to diagnose and treat them even to the experienced pathologists.

    CASE PRESENTATION: The featured case describes a 40-year-old male who presented with symptoms suggestive for sinusitis. Further diagnostic investigation by the functional endoscopic sinus surgery (FESS) revealed a chronic sinusitis with multiple biopsies showing negative for malignancy, viral and bacterial infections and therefore undiagnosed for sinonasal NK/T-cell lymphoma. Subsequently after a month of surgery, he developed multiple lymph nodes in inguinal where biopsy revealed extranodal NK/T-cell non-Hodgkin lymphoma, high grade but in no time for treatment, he finally succumbed to the illness.

    CONCLUSION: The case presented here was initially diagnosed as a chronic sinusitis, not as sinonasal NK/Tcell lymphoma which later developed into extranodal NK/T-cell lymphoma. The prognosis showed improvement for nasal lymphomas but remains poor for disseminated and extranasal lymphomas which are more aggressive with lower survival rate. It is clinically important to differentiate diseases for proper staging and monitoring as they require completely different treatment strategies.

    Matched MeSH terms: Nose Neoplasms/diagnosis*
  6. Ismail F, Peyman M, Waran V, Vasudevan S, Subrayan V
    Optom Vis Sci, 2015 Apr;92(4 Suppl 1):S33-5.
    PMID: 25730333 DOI: 10.1097/OPX.0000000000000528
    To report a rare case of nasal chondroma presenting as hypertelorism.
    Matched MeSH terms: Nose Neoplasms/diagnosis*
  7. Fadzilah I, Salina H, Khairuzzana B, Rahmat O, Primuharsa Putra SH
    Ear Nose Throat J, 2014 Jun;93(6):E33-5.
    PMID: 24932827
    Schwannomas of the nasal cavity and paranasal sinuses are quite rare, especially in the nasal vestibule. We report the case of a 61-year-old woman who presented with a 2-month history of progressively worsening right-sided epistaxis and nasal blockage. Rigid nasoendoscopy showed a mobile, smooth, globular mass occupying the right nasal vestibule. The mass arose from the lateral nasal wall and impinged on the anterior part of the middle turbinate posteriorly. Computed tomography of the paranasal sinuses showed a 3.8 × 1.7-cm enhancing mass in the right nostril. The mass obliterated the nasal cavity and caused mild deviation of the septum. The preoperative histopathologic examination showed positivity for vimentin and S-100 protein, suggesting a diagnosis of schwannoma. The patient underwent an intranasal laser-assisted excision biopsy. The histopathologic examination confirmed the diagnosis of schwannoma. Postoperative recovery was uneventful, and no recurrence was seen in the follow-up period.
    Matched MeSH terms: Nose Neoplasms/diagnosis*
  8. Saleh KA, Razif, Gendeh BS
    Med J Malaysia, 2011 Jun;66(2):160-1.
    PMID: 22106705
    Extra nodal NK/T cell lymphoma, 'nasal type' is a rare clinicopathological entity. The prevalence of nasal lymphoma is estimated at 0.17-1.5% for all non -Hodgkin's lymphomas (NHL), of which 45% originate from the NK/T cell. It is more commonly encountered in Asian countries. The main clinical features are nasal congestion and epistaxis due to local aggressive destruction. It has a distinct immunophenotypic profile of CD2+, CD56+ and CD3-. The tumor often shows polymorphic lymphoreticular infiltrates and necrosis. We present a case of a 50-year-old male who presented with lateral nasal wall infection following endoscopic sinonasal surgery and later proven to be extranodal NK/T cell 'nasal type' lymphoma with immunophenotypic features.
    Matched MeSH terms: Nose Neoplasms/diagnosis*
  9. Shahrizal TA, Prepageran N, Rahmat O, Mun KS, Looi LM
    Ear Nose Throat J, 2009 Feb;88(2):786-9.
    PMID: 19224479
    Extramedullary plasmacytoma is a rare plasma cell proliferative disorder with a predilection for the head and neck region. Occasionally, it presents as a solitary lesion in the nasal cavity. We report a case of an isolated lesion in the middle turbinate of the right nasal cavity. The lesion was completely excised via an endoscopic approach. We also review the pathology and management of plasmacytomas in general.
    Matched MeSH terms: Nose Neoplasms/diagnosis*
  10. Vikneswaran T, Gendeh BS, Tan VES, Phang KS, Saravanan K
    Med J Malaysia, 2005 Oct;60(4):485-8.
    PMID: 16570712
    Hemangiopericytoma is a very rare angiogenic tumor. In the nasal cavity, it can be considered malignant. It occurs in various parts of the body but those in the nasal cavity account for only 5% of total cases. Less than 200 cases have been reported worldwide involving the nose and paranasal sinuses. Due to its rarity a proper line of management has not been established to tackle this tumour. This article highlights two cases of hemangiopericytoma (HPC), one in an adult and the other in a child, presenting as an intranasal mass.
    Matched MeSH terms: Nose Neoplasms/diagnosis*
  11. Kenali MS, Fadzilah I, Maizaton AA, Sani A
    Med J Malaysia, 2004 Mar;59(1):108-11.
    PMID: 15535345
    A 31 years old Chinese male with acquired immunodeficiency syndrome (AIDS) presented with concurrent mycobacterial infection and a synchronous non-Hodgkin's lymphoma of the nose. The diagnoses were made over a period of two months. Treatment for the mycobacterial infection was administered but he succumbed to the disease shortly after the diagnosis of NHL was established. This was an unusual case where two pathologies occurred in the same site in a patient with AIDS.
    Matched MeSH terms: Nose Neoplasms/diagnosis
  12. Tan J, Said H, Chong SM
    Med J Malaysia, 1988 Mar;43(1):49-54.
    PMID: 3244320
    Matched MeSH terms: Nose Neoplasms/diagnosis
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