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1.
Indian J Pathol Microbiol ; 60(4): 469-474, 2017.
Article in English | MEDLINE | ID: mdl-29323057

ABSTRACT

INTRODUCTION: Breast cancer is the commonest cause of death among middle aged women. BRCA1 associated tumors carry a poor prognosis. Angiogenesis is considered necessary for tumor growth and for its metastasis. Hypoxia stimulates HIF-1α which then activates transcription of various proangiogenic cytokines like VEGF. In the present study we examined HIF-1α expression, sVEGF levels and BRCA1 mutations and their relation with clinicopathological parameters. We also determined whether the angiogenic markers have different role in angiogenesis in BRCA1 related cancers as compared to sporadic breast cancers. MATERIALS AND METHODS: The study was conducted on 50 cases of breast cancer specimens. Histopathological typing and grading was done followed by immunohistochemistry for BRCA1 and HIF-1α. VEGF was done in the serum by ELISA. RESULTS: All the tumors were infiltrating ductal carcinoma NOS. 16 cases were reported grade II and 34 cases as grade III. On immunohistochemistry, 27 cases showed BRCA1 positivity and HIF-1α was positive in 39 cases. sVEGF levels were increased in 21 cases (42%). BRCA1 positivity, HIF-1α expression and increased VEGF levels were significantly associated with higher grade and lymph node metastasis. There was significant correlation of BRCA1 positivity with increased HIF-1α expression (P = 0.009) and increased sVEGF levels (P = 0.005). CONCLUSION: Our findings suggest that BRCA 1 positive tumors have unique molecular profile and different mechanism of tumorigenesis. Such tumors are associated with increased HIF-1α expression and VEGF levels.


Subject(s)
BRCA1 Protein/genetics , Breast Neoplasms/pathology , Hypoxia-Inducible Factor 1, alpha Subunit/analysis , Mutation , Vascular Endothelial Growth Factor A/analysis , Adult , Aged , Biomarkers, Tumor/analysis , Female , Histocytochemistry , Humans , Immunohistochemistry , Microscopy , Middle Aged , Prospective Studies , Tertiary Care Centers
2.
Iran J Pathol ; 11(2): 161-6, 2016.
Article in English | MEDLINE | ID: mdl-27499779

ABSTRACT

Chondrosarcoma is a mesenchymal tumor composed of tumor cells producing cartilage. It is more common in older age and often affects the axial skeleton. We report a rare case of chondrosarcoma mimicking a sellar and suprasellar mass with parasellar extension. A 40 yr woman presented with decreasing visual acuity and headache. Magnetic resonance (MR) image revealed a cystic sellar and suprasellar mass with parasellar extension showing mild enhancing solid component. It favored the diagnosis of craniopharyngioma. The patient underwent trans-sphenoidal partial resection of the tumor resulting in removal of the sellar mass. However, the suprasellar mass could not be excised completely due to limited surgical field. The pathologic diagnosis was chondrosarcoma. Eight months after the operation, pterional approach was performed to remove the remaining mass. Intraoperative findings confirmed that the mass originated from dorsum sellae.

3.
Skinmed ; 10(2): 116-8, 2012.
Article in English | MEDLINE | ID: mdl-22545332

ABSTRACT

A 16-year-old young man presented with intensely itchy erythematous dermatitis on the body for 1 week and vesicular lesions on the palms and soles for 4 to 5 days. Lesions on the palms and soles were accompanied by severe burning and itching. The patient gave a history of sore throat and fever, 1 week prior to the onset of lesions. A general physical examination was normal, and cutaneous examination revealed multiple, well-defined erythematous scaly plaques with collaret scaling on the trunk and extremities (Figure 1). Vesicular lesions were seen on the palms and soles (Figure 2). The differential diagnoses we considered were pityriasis rosea and secondary syphilis. The possibility of dermatophytid, vesicular pityriasis rosea, and pompholyx was limited to the palms and sole lesions. Complete blood cell count was within normal limits. Results from antistreptolysin O titer, potassium hydroxide mount, and venereal disease research laboratory were negative. Skin biopsies were taken from the back and left palm. The biopsy specimen from the back revealed focal spongiosis, lymphocyte exocytosis, vacuolar changes in the basal layer, and perivascular lymphocytic infiltrate in the dermis (Figure 3). The biopsy obtained from the vesicular lesion on the left palm revealed an intraepidermal vesicle with no evidence of acantolytic process (Figure 4). A diagnosis of pityriasis rosea was made and the patient was started on clarithromycin 500 mg once a day for 7 days, along with antihistamines and emollients. The lesions faded dramatically in a very short period, and there was significant involution of almost all of the lesions after 7 days of clarithromycin. During the 6 months of follow-up, no recurrence was observed.


Subject(s)
Eczema, Dyshidrotic/pathology , Pityriasis Rosea/pathology , Adolescent , Anti-Bacterial Agents/therapeutic use , Clarithromycin/therapeutic use , Humans , Male , Pityriasis Rosea/diagnosis , Pityriasis Rosea/drug therapy
4.
Int J Appl Basic Med Res ; 1(1): 54-6, 2011 Jan.
Article in English | MEDLINE | ID: mdl-23776775

ABSTRACT

Ameloblastic carcinoma (AC) is a rare epithelial odontogenic tumor of the jaws, which exhibits cytological features of ameloblastoma and carcinoma. It has a distinct predilection for mandible. These lesions may initially show histologic features of ameloblastoma that dedifferentiate over time. Others may present with features of epithelial dedifferentiation in ameloblastoma. A case of ameloblastomic carcinoma in a 64-year-old male is reported, who presented with swelling in the left mandible 3 months after the extraction of the left upper molar.

5.
Acta Cytol ; 54(5 Suppl): 1035-8, 2010.
Article in English | MEDLINE | ID: mdl-21053594

ABSTRACT

BACKGROUND: Hodgkin's lymphoma (HL) is a malignant neoplasm of lymphoid tissues. Cervical lymphadenopathy is the most common head and neck presentation for HL. Although uncommon, extranodal HL observed at the time of diagnosis is well documented and is typically associated with generalized disease or local spread from adjacent lymph nodes. Primary osseous HL is very rare. CASE: A 23-year-old male presented with a solitary vertebral lesion as primary manifestation of HL. CONCLUSION: HL should be remembered in the differential diagnosis of lytic lesions, especially involving the vertebrae and pelvic bones.


Subject(s)
Hodgkin Disease/diagnosis , Hodgkin Disease/pathology , Spinal Neoplasms/pathology , Biopsy, Fine-Needle , Humans , Male , Radiography , Reed-Sternberg Cells/pathology , Spine/diagnostic imaging , Spine/pathology , Young Adult
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