Displaying all 19 publications

Abstract:
Sort:
  1. Azahsyahrina, A., Moonyza, A., Lee, B.R., Fazarina, M.
    Medicine & Health, 2017;12(1):109-112.
    MyJurnal
    Epidermal naevus is a congenital cutaneous hamartoma with a benign course. We highlight a rare case of epidermal naevus with concurrent basal cell carcinoma. A 79-year-old male had a skin biopsy at our centre for an enlarging skin nodule within a linear papular lesion measuring 2 x 4 cm at the left side of his neck, which was later diagnosed as basal cell carcinoma arising from an epidermal naevus. PIK3CA mutation is attributed to basal cell carcinoma which suggests the basal cell carcinoma component is independent of the epidermal naevus component. Clinicians and pathologists must be aware of possible malignant changes that might arise in an epidermal naevus.
    Keywords: basal cell carcinoma, BCC, epidermal naevus
    Matched MeSH terms: Nevus*
  2. Gupta A, Srilatha PS, Suvarna N, Rao L
    Indian J Pathol Microbiol, 2011 Jan-Mar;54(1):156-7.
    PMID: 21393904 DOI: 10.4103/0377-4929.77384
    Deep penetrating nevus (DPN) is a variant of melanocytic nevus which goes unrecognized due to its relative rarity and may be misinterpreted as malignant melanoma. It commonly presents in young adults as a dark pigmented lesion on the face, neck, or shoulder. A 60-year-old lady presented with a mole over the left arm of 8 years duration. A biopsy of the lesion was performed under the clinical impression of a compound nevus with suspicion of malignancy. Based on the histologic features, a diagnosis of DPN was put forward.
    Matched MeSH terms: Nevus, Pigmented/diagnosis*; Nevus, Pigmented/pathology*
  3. Manley S
    J Gen Intern Med, 2018 10;33(10):1822-1823.
    PMID: 29968052 DOI: 10.1007/s11606-018-4549-9
    Matched MeSH terms: Nevus, Pigmented/psychology; Nevus, Pigmented/surgery*
  4. Pang EB, Pang KP
    Med J Malaysia, 2015 Jun;70(3):198-9.
    PMID: 26248784
    Melanoma of the ear canal is extremely rare; due to its hidden area, most would present late in their history. We present the first case reported, of a black pigment foreign body mimicking a melanoma in the external auditory canal. A 14 year old Chinese male presented with right sided otalgia and itch. Otoscopic examination revealed an irregular black naevus in the right auditory canal. An intraoperative excision showed a black pigment foreign body giant cell reaction. Clinicians should be aware of the possibility of a foreign body granuloma of the ear canal that might mimic a melanoma.
    Matched MeSH terms: Nevus; Nevus, Pigmented
  5. Bhullar A, Shamsudin N
    N Engl J Med, 2015 Jun 25;372(26):2541.
    PMID: 26107054 DOI: 10.1056/NEJMicm1406555
    Matched MeSH terms: Nevus/pathology*
  6. Kandiah R, Sukumaran K, Chandran S, Jayalakshmi P
    Med J Malaysia, 1988 Jun;43(2):178-80.
    PMID: 3237135
    Matched MeSH terms: Nevus, Pigmented/pathology*
  7. Yatiee SL, Mohd Khairi MD, Md Salzihan MS, Ikmal HB
    Med J Malaysia, 2018 04;73(2):121-122.
    PMID: 29703880 MyJurnal
    The incidence of intradermal nevus in the external auditory canal is uncommon. We herein are describing a case of 60-year-old lady who presented with foreign body sensation in the right external ear canal (EAC) with mild discomfort and ear bleed during ear picking. Otoscopic examination revealed hyperpigmented mass on the floor of the outer two third of EAC. Complete excisional biopsy of the mass resulted in histopathology findings of intradermal nevus. Despite the fact that the disease is not alarming, the possibilities of benign melanocytic nevi transformation into malignant lesions such as melanoma need to be ruled out.
    Matched MeSH terms: Nevus, Pigmented; Nevus, Intradermal
  8. Yap FB
    Singapore Med J, 2009 May;50(5):e161-2.
    PMID: 19495497
    Nevus lipomatosus superficialis is a rare benign skin malformation characterised by ectopic adipocytes in the upper dermis. It is classified into two types: a classical Hoffman-Zurhelle type and the solitary type. A case of the classical type with multiple soft, non-tender, pedunculated, cerebriform, skin-coloured papules and nodules over the right lower back is presented in a 21-year-old Malay woman. She had a rare occurrence of ulceration and necrosis of the lesions.
    Matched MeSH terms: Nevus, Pigmented/diagnosis; Nevus, Pigmented/pathology; Nevus, Pigmented/surgery
  9. Singh M, Kaur B, Annuar NM
    Br J Ophthalmol, 1988 Feb;72(2):131-3.
    PMID: 3349013
    A rare case of choroidal malignant melanoma in a naevus of Ota is described. This is the first reported case from Asia outside the Japanese population. This case illustrates the need for close observation of all pigmented lesions of the eye.
    Matched MeSH terms: Nevus of Ota/pathology*; Nevus, Pigmented/pathology*
  10. Wong JG, Lai XJ, Sarafian RY, Wong HS, Smith JB
    Retin Cases Brief Rep, 2016;10(3):221-4.
    PMID: 26509999 DOI: 10.1097/ICB.0000000000000233
    PURPOSE: Choroidal nevus is the most common ocular fundus tumor in adults. Previous studies have widely discussed the features of choroidal neovascularization secondary to nevus and its treatment options. Polypoidal choroidal vasculopathy (PCV) is an exudative chorioretinopathy that is often underdiagnosed. Clinical features, natural history, and treatment response of PCV are distinct from occult choroidal neovascularization. Polypoidal choroidal vasculopathy secondary to choroidal nevus has not been previously documented. We report a patient with a history of stable choroidal nevus who developed a polypoidal lesion at the edge of the nevus lesion.

    METHODS: A white woman who presented with a choroidal nevus and clinical features of PCV was examined using fundoscopy, optical coherence tomography, fluorescein angiography, and indocyanine green angiography.

    RESULTS: A polypoidal lesion with an associated branching vascular network adjacent to the nevus was demonstrated by optical coherence tomography, fluorescein angiography, and indocyanine green angiography. The patient was asymptomatic and was managed conservatively.

    CONCLUSION: Our case showed that PCV developing in association with a stable choroidal nevus. Pathogenic mechanisms of this condition may include chronic degenerative or inflammatory changes at the level of the retinal pigment epithelium resulting in vascular changes. Unlike treatment of occult choroidal neovascularization secondary to nevus, optimal management of PCV secondary to nevus may vary. Indocyanine green angiography is the gold standard for the diagnosis of PCV and is a useful investigation in atypical choroidal neovascularization.

    Matched MeSH terms: Nevus/complications*; Nevus/pathology
  11. Goh EH, Zarina AL, Thambidorai CR, Maizaton AA, Siti AM, Somasundram S
    Pediatr Surg Int, 2008 Apr;24(4):447-9.
    PMID: 17437116
    The diagnosis of malignant melanoma (MM) in children is difficult due to its uncommon occurrence as well histological similarities to Spitz nevus. A case of MM of the foot in an 11-year-old boy is reported illustrating the histological overlap between Spitz nevus and MM. In our patient, both the primary foot lesion and the regional inguinal metastases were amelanotic, further increasing the diagnostic difficulty. The literature on MM in children is limited and the documentation of such unusual cases is necessary to improve the knowledge on this disease.
    Matched MeSH terms: Nevus, Epithelioid and Spindle Cell/pathology*; Nevus, Epithelioid and Spindle Cell/surgery
  12. Wong JG, Lai XJ, Sarafian RY, Wong HS, Smith JB
    Int Med Case Rep J, 2017;10:51-54.
    PMID: 28243154 DOI: 10.2147/IMCRJ.S107648
    We report a case of a Caucasian female who developed active polypoidal choroidal vasculopathy (PCV) at the edge of a stable choroidal nevus and was successfully treated with verteporfin photodynamic therapy. No active polyp was detectable on indocyanine green angiography 2 years after treatment, and good vision was maintained. Indocyanine green angiography is a useful investigation to diagnose PCV and may be underutilized. Unlike treatment of choroidal neovascularization secondary to choroidal nevus, management of PCV secondary to nevus may not require intravitreal anti-vascular endothelial growth factor therapy. Photodynamic monotherapy may be an effective treatment of secondary PCV.
    Matched MeSH terms: Nevus
  13. Wong SW, Kyaw L, Ong LC, Zulfiqar AM
    J Paediatr Child Health, 2011 Apr;47(4):237-9.
    PMID: 20500432 DOI: 10.1111/j.1440-1754.2010.01739.x
    Sturge-Weber syndrome is a neurocutaneous syndrome characterised by facial port wine stain, ipsilateral leptomeningeal angioma and vascular eye abnormalities. We report a rare case of Sturge-Weber syndrome without facial nevus presenting with neonatal seizures.
    Matched MeSH terms: Nevus*
  14. Kanaheswari Y, Hamzaini AH, Wong SW, Zulfiqar A
    Acta Paediatr, 2008 Nov;97(11):1589-91.
    PMID: 18671691 DOI: 10.1111/j.1651-2227.2008.00971.x
    Phakomatosis pigmentovascularis (PPV) is a rare congenital syndrome characterized predominantly by cutaneous vascular malformations and pigmentary naevi. The most frequently reported form, Type II b, is associated with systemic involvement. Sturge-Weber Syndrome (SWS) with concomitant glaucoma, Klippel-Trenaunay Syndrome (KTS) and naevus of Ota have been frequently described, but there have only been two case reports with asymptomatic renal anomalies.
    Matched MeSH terms: Nevus of Ota/complications
  15. Ling KC, Couper NTA, Hu WS
    Med J Malaysia, 1984 Jun;39(2):173-6.
    PMID: 6513859
    A relatively uncommon case of Gorlin's syndrome is reported. The jaw cysts led to the diagnosis of Gorlin's syndrome in the patient.
    Matched MeSH terms: Basal Cell Nevus Syndrome/diagnosis*
  16. Mat Johar F, Wan Sulaiman WA, Mat Saad AZ, Basiron N, Sahid NA
    Int J Surg Case Rep, 2020;72:202-206.
    PMID: 32544829 DOI: 10.1016/j.ijscr.2020.05.036
    INTRODUCTION: Blue Rubber Bleb Nevus Syndrome (BRBNS) also known as Bean's Syndrome is an atypical type of vascular malformation. To date, around 200 cases have been reported world-wide. In view of its low incidence rate, clinicians might misdiagnose and under treat. The key features of this syndrome are characterized by multiple cutaneous, soft tissue and gastrointestinal tract venous malformations.

    PRESENTATION OF CASE: We report the first case of Blue Rubber Bleb Nevus Syndrome in Malaysia, a 23 years old Malay girl who suffers from multiple cutaneous venous malformation and gastrointestinal bleeding episodes.

    DISCUSSION: The typical morbidity for this syndrome is symptomatic anemia due to secondary iron deficiency due to the gastrointestinal venous malformation bleeding. In managing the gastrointestinal bleeding, it mainly depends on the severity of gastrointestinal bleeding, some may resolve spontaneously, while the others may be needing blood transfusion, and some may require GIT resections. As for cutaneous lesions, normally it is innocuous depending on the region and size. Large or problematic cutaneous venous malformation might benefit from sclerotherapy or excision.

    CONCLUSION: Multidisciplinary approach is crucial in managing BRBNS case due to its complexity and the spectrum of multiple organ involvement to ensure the best outcome to the patient.

    Matched MeSH terms: Nevus; Nevus, Blue
  17. Arshad AR, Azman WS, Kreetharan A
    Head Neck, 2008 Apr;30(4):544-8.
    PMID: 17972311 DOI: 10.1002/hed.20708
    BACKGROUND: Sebaceous nevus is a benign congenital epidermal nevus. Its association with basal cell carcinoma is well known.
    METHOD: This is a case report of sebaceous carcinoma complicated by both basal cell carcinoma and squamous cell carcinoma.
    RESULTS: The behavior of this tumor is very aggressive, resulting in poor prognosis.
    CONCLUSIONS: All sebaceous nevi should be excised early.
    Matched MeSH terms: Nevus, Sebaceous of Jadassohn/pathology*; Nevus, Sebaceous of Jadassohn/surgery
  18. Chooi LK, Saad AZM, Durairajanayagam S
    Indian J Plast Surg, 2017 6 16;50(1):104-106.
    PMID: 28615821 DOI: 10.4103/ijps.IJPS_25_17
    Malignant melanoma is a potentially lethal cutaneous malignancy. Melanoma in paediatrics is rare as compared to adult melanoma. The clinicopathological characteristics of paediatric melanoma are different from adult melanoma, and the presence of melanoma mimics which occurs frequently in children (Spitz naevi) resulted in diagnosis uncertainty. We reported a 9-year-old girl who presented with a slow-growing, pyogenic granuloma-like lesion which was diagnosed with melanoma. It is important to have a high index of suspicion in paediatric skin lesion that would usually be deemed benign. Early tissue biopsy in a suspicious lesion prevents delayed diagnosis and treatment.
    Matched MeSH terms: Nevus, Epithelioid and Spindle Cell
  19. Chow HT
    PMID: 9830650
    The odontogenic keratocyst has been well documented and extensively studied. It is of particular interest because of its high recurrence rate and aggressive nature. The material for this study consisted of 70 cases of odontogenic keratocysts in predominantly ethnic Chinese patients who were treated from 1981 to 1996. The cases were retrospectively studied to compare characteristics of the lesion in this population with those in previous reports. Most of the patients in this series were 21 to 30 years of age. Association with an impacted mandibular third molar was found in more than 50% of the cases. The recurrence rate was 20% for 35 patients with a follow-up period of at least 5 years. The follow-up period for the whole series ranged from 1 to 16 years. Treatment was surgical enucleation with peripheral ostectomy. There were no significant differences in characteristics with respect to presentation and prognosis between this series and those described in previous publications.
    Matched MeSH terms: Basal Cell Nevus Syndrome/complications
Filters
Contact Us

Please provide feedback to Administrator (afdal@afpm.org.my)

External Links