Displaying publications 221 - 240 of 5116 in total

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  1. Nah SH, Marks SC, Subramaniam K
    Lepr Rev, 1985 Mar;56(1):51-5.
    PMID: 3990507
    Matched MeSH terms: Alveolar Process/pathology*; Leprosy/pathology*; Maxilla/pathology*
  2. Sivanesan S, Chandran S
    Med J Malaysia, 1982 Sep;37(3):257-60.
    PMID: 6294490
    Three consecutive cases of lacrimal gland carcinoma seen at the University Hospital during a twelve-year period are presented. One case was unusual, presenting at the age of sixteen years and developing metastases to the lungs. Adenoid cystic carcinoma is the commonest type of lacrimal malignancy and its clinico-pathological features and surgical management are discussed.
    Matched MeSH terms: Carcinoma, Adenoid Cystic/pathology*; Eye Neoplasms/pathology*; Lacrimal Apparatus Diseases/pathology*
  3. Siar CH, Ng KH, Chia TY
    Singapore Dent J, 1990 Dec;15(1):35-7.
    PMID: 2097728
    Granular cell ameloblastomas are uncommon lesions accounting for about 3-5% of all histologic subtypes of ameloblastoma. The plexiform granular cell odontogenic tumour, on the other hand, is a newly described lesion characterised by a monophasic plexiform pattern of granular cells. This article reports a tumour found occurring in the left mandible of a 67-year-old Indian male which histologically showed features of both the aforementioned lesions.
    Matched MeSH terms: Ameloblastoma/pathology*; Mandibular Neoplasms/pathology*; Odontogenic Tumors/pathology*
  4. Siar CH, Jalil AA, Ram S, Ng KH
    J Oral Sci, 2004 Mar;46(1):51-3.
    PMID: 15141724
    Osteoma is a benign tumour consisting of mature bone tissue. It is an uncommon lesion that occurs mainly in the bones of the craniofacial complex. Only a few cases involving the condylar process have been reported. An osteoma of the left condyle causing limited mouth-opening in a 32-year-old Malaysian Chinese female is reported here to alert the practitioner to consider this lesion as a diagnostic possibility in instances of trismus or limited-mouth opening.
    Matched MeSH terms: Mandibular Condyle/pathology*; Mandibular Neoplasms/pathology; Osteoma/pathology
  5. George-Kodiseri E, Faridah K, George-Vadaketh R, Lau PS, Ong MS, Tan TY, et al.
    Family Physician, 1989;1:34-42.
    Matched MeSH terms: Pathology
  6. George E, Wong HB
    Family Physician, 1993;5:42-46.
    Matched MeSH terms: Pathology
  7. Leung AKC, Leong KF, Barankin B
    J Pediatr, 2019 07;210:232.
    PMID: 31003749 DOI: 10.1016/j.jpeds.2019.03.013
    Matched MeSH terms: Mouth Floor/pathology; Telangiectasia, Hereditary Hemorrhagic/pathology*; Tongue/pathology
  8. Wang S, Xu W, Li LF
    Pediatr Infect Dis J, 2017 Sep;36(9):912-914.
    PMID: 28338526 DOI: 10.1097/INF.0000000000001593
    Cutaneous larva migrans is a frequent dermatologic problem among travelers in tropical areas, but its association with Löffler's syndrome is an extremely rare condition, particularly in children. Here, we describe a 6-year-old boy presenting cutaneous larva migrans associated with Löffler's syndrome.
    Matched MeSH terms: Foot/pathology; Leg/pathology; Lung/pathology
  9. Arshad AR
    Cleft Palate Craniofac J, 1995 Mar;32(2):167-9.
    PMID: 7748879
    Midline cleft of the lower lip is defined as a midline vertical cleft of the soft tissue of the lower lip. It may present with a midline cleft of the mandible. It may also be accompanied by other congenital anomalies such as a cleft tongue, ankyloglossia, a heart lesion, and absence of the hyoid bone. The etiologic cause is thought to be a failure of mesodermal penetration into the midline structures of the first branchial arch. This case report is on a female child who presented with an incomplete midline cleft of the soft tissue of the lower lip. It was surgically corrected with a vertical wedge excision and primary closure.
    Matched MeSH terms: Branchial Region/pathology; Lip/pathology; Mesoderm/pathology
  10. Cirielli V, Bortolotti F, Cima L, De Battisti Z, Del Balzo G, De Salvia A, et al.
    Med Sci Law, 2021 Jan;61(1_suppl):25-35.
    PMID: 33591882 DOI: 10.1177/0025802420965763
    The magnitude of the diagnostic benefit conferred by performing histopathological examinations after medico-legal/forensic autopsies remains debatable. We have tried to address this issue by reviewing a series of histopathology referrals concerning medico-legal autopsies in real-world routine practice. We present an audit of the consultations provided to forensics by clinical pathologists at our institute between 2015 and 2018. Over this period, 493 post-mortem examinations were performed by forensic pathologists. Of these cases, 52 (11%) were referred for histopathology. Gross assessment was requested in 22/52 (42%) cases. Histopathology examination was performed on single organs in 15/52 (29%) cases, primarily on the lung and heart, whereas parenchymatous multi-organ analysis was carried out in 14/52 (27%) cases. Bone-marrow sampling was studied in 4/52 (8%) cases. Immunohistochemistry was needed in 16/52 (31%) cases, special stains in 9/52 (21%) cases and molecular analysis in 4/52 (8%) cases. Focusing on technical processes, standard methodology on pre-analytical procedures was changed in 10/52 (19%) cases in order to answer specific diagnostic questions. We showed that although most of the time the diagnosis is clear by the end of dissection on the basis of the macroscopic findings, histopathology can provide, modify or confirm the cause of death in many medico-legal/forensic cases. Therefore, it is desirable that forensic pathologists and clinical pathologists establish robust working relationships in a cooperative environment. We conclude that it is important to implement guidelines based on real-world routine practice in order to identify cases where histopathology can provide useful contributions, which in our experience applied to 11% of forensic cases.
    Matched MeSH terms: Pathology, Clinical/methods*; Forensic Pathology/methods*
  11. Alturkustani M, Bahakeem B, Zhang Q, Ang LC
    Malays J Pathol, 2020 Aug;42(2):187-194.
    PMID: 32860370
    INTRODUCTION: Multiple sclerosis (MS) has variable clinical presentations, prognoses, pathogeneses, and pathological patterns. We conducted a pathological review of acute MS-associated lesions that focused on the degree of axonal injury, myelin loss, and glial reaction to determine whether the observed demyelination was of the primary or secondary type.

    MATERIALS AND METHODS: After searching the records for a 15-year period at the London Health Sciences Centre Pathology Department, we identified 8 cases of surgical acute lesion biopsies in which clinical MS diagnoses were made before or after the biopsy.

    RESULTS: The white matter pathologies in these cases could be sorted into 3 morphological patterns. The first pattern, which represents typical demyelinated plaques, was observed in 4 cases and was characterised by nearly complete demyelination accompanied by variable degrees of axon preservation and axonal swelling. The second pattern was observed in 3 cases and was characterised by demyelinating lesions containing variable numbers of myelinated axons mixed with a few demyelinated axons and variable numbers of axonal swellings. The myelinated axons ranged from scattered fibres to bands of variable thickness, and the demyelination was a mixture of primary and secondary demyelination. The third pattern was observed in 1 case and was characterised by well-demarcated areas of reduced myelin staining and numerous apoptotic nuclei. Axonal staining revealed many fragmented axons with reduced myelin staining but no definitely demyelinated axons.

    CONCLUSIONS: This report shows that the predominant pathology underlying acute MS-related lesions is not limited to demyelination but can include axonal degeneration alone or in combination with primary demyelination which reflect different pathogenesis for these acute lesions.

    Matched MeSH terms: Axons/pathology; Multiple Sclerosis/pathology*; White Matter/pathology*
  12. Mohamad MA, Jarmin R, Md Pauzi SH
    Malays J Pathol, 2020 Dec;42(3):455-459.
    PMID: 33361729
    Schwannomas are mesenchymal tumors that are characteristically benign and slow growing, which originate from any nerve with Schwann cell sheath. Gastrointestinal schwannomas are rare with distinct morphologic features as compared to schwannomas of soft tissue or central nervous system. A 77-year-old male patient was diagnosed with gastrointestinal stromal tumor based on radiological findings and clinical impression when he presented with worsening abdominal discomfort and pain. He underwent distal gastrectomy however histopathological examination of the tumour revealed schwannoma. This case report presents a rare case of a symptomatic gastric schwannoma, whose definitive diagnosis was established by histopathological and immunohistochemical findings postoperatively.
    Matched MeSH terms: Neurilemmoma/pathology*; Stomach Neoplasms/pathology*; Gastrointestinal Stromal Tumors/pathology
  13. Sharma, Shobha, Haryani Harun, Rahayu Mustaffa Kamal, Srinovianti Noerdin
    MyJurnal
    This study in the management of dysphagia or swallowing disorders involved 72 contactable Speech-Language Pathologists (SLP) in Malaysia. A survey was undertaken to identify the patterns of dysphagia management by SLPs in Malaysia by identifying the percentage of SLPs in Malaysia who have managed swallowing disorders, the approximate number of patients, assessment and therapy techniques used, other professional involvement and the factors that influenced the confidence levels of the SLPs in managing swallowing disorders. Fifty percent (50%) of the forty four SLPs (61.6%) who responded to the survey had previously managed swallowing disorders. It was estimated that 5% (430 of 8268) of patients referred to the SLPs in Malaysia presented with dysphagia and were subsequently managed for their swallowing problems. The oromotor examination was carried out most frequently (100%) for evaluation of dysphagia while the compensatory technique proved to be the most frequently used management technique (77.3%). Most referrals to the SLPs were received from the neurosurgeon (59.1%); the otorhinolaryngologist was most referred to by the SLPs (50%). By using the Chi-squared analysis, it was found that clinical training in dysphagia at the undergraduate or post-graduate levels influenced the confidence levels of the SLPs in managing dysphagia cases (χ2 = 10.063 with p value = 0.007).
    Matched MeSH terms: Speech-Language Pathology
  14. Ho CS, Horiuchi T, Taniguchi H, Umetsu A, Hagisawa K, Iwaya K, et al.
    Biomed Eng Online, 2016 Aug 20;15(1):98.
    PMID: 27542354 DOI: 10.1186/s12938-016-0220-z
    Composition of atherosclerotic arterial walls is rich in lipids such as cholesterol, unlike normal arterial walls. In this study, we aimed to utilize this difference to diagnose atherosclerosis via multispectral fluorescence imaging, which allows for identification of fluorescence originating from the substance in the arterial wall.
    Matched MeSH terms: Aorta, Abdominal/pathology; Coronary Vessels/pathology; Atherosclerosis/pathology
  15. Chong KC
    Postgrad Med J, 1976 Aug;52(610):504-10.
    PMID: 824633
    The incidence, clinical features and pathology of nine cases of diverticula of the appendix in Malaysians are reported. The findings are discussed and compared with those previously reported. The pathogenesis of the lesion in eight cases is unknown. The rare association of lumenal obstruction by a carcinoid tumour and diverticulum formation in the appendix is seen in one case.
    Matched MeSH terms: Appendiceal Neoplasms/pathology; Appendix/pathology*; Diverticulum/pathology*
  16. Murugasu R, Dissanaike AS
    Trans R Soc Trop Med Hyg, 1973;67(6):880.
    PMID: 4788765
    Matched MeSH terms: Liver/pathology; Mesentery/pathology; Pancreas/pathology
  17. Dutt AK, Krishnan M, Lim EJ
    Med J Malaya, 1969 Sep;24(1):74-8.
    PMID: 4243848
    Matched MeSH terms: Bronchial Diseases/pathology*; Cryptococcosis/pathology*; Lung Diseases, Fungal/pathology*
  18. Pallie W, Manuel JK
    Med J Malaya, 1968 Dec;23(2):96-7.
    PMID: 4240828
    Matched MeSH terms: Ganglia, Spinal/pathology*; Intervertebral Disc Displacement/pathology*; Spinal Cord/pathology*
  19. Tan GC, Prasad V
    Int. J. Surg. Pathol., 2018 Feb;26(1):34.
    PMID: 28508688 DOI: 10.1177/1066896917709946
    Matched MeSH terms: Kidney/pathology*; Kidney Neoplasms/pathology*; Wilms Tumor/pathology*
  20. Chaubal TV, Bapat R, Poonja K
    Am J Med, 2017 10;130(10):e451.
    PMID: 28528920 DOI: 10.1016/j.amjmed.2017.04.026
    Matched MeSH terms: Exostoses/pathology*; Mandible/pathology; Palate, Hard/pathology
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