Page 13 - ACCF Essentia | Vol. III | Issue 3 | June 2024
P. 13

Primary heterotopic Menin
         Primary heterotopic Meningioma of Nasal
                                    g
                                      ioma of Nasal
         Cavity
         Cavity
                           g
         Extracranial meningiomas are relatively
         Extracranial meningiomas are relatively
         uncommon (comprise 1-2% of the
         uncommon (comprise 1-2% of t   he
         meningiomas). In the head and neck region,
         meni ng iomas ) . In the head and neck r eg ion,

                     i
                        i
                        nonasal tract,
                                       p
                     n s
                                         i
                                        r
         pa
                                         ma
                                             ry
         particularly in sinonasal tract, primary
             cular
                  ly
           rt
             i
                          ng
                             i
                         i
                             oma needs to be
                   i
         heterotop
         heterotopic meningioma needs to be
                   c men
         distinguished from other common tumours of
         distinguished from other common tumours of
                        s pat
                       i
                 i
                                              th a mass
                                             i
         that region. This patient presented with a mass
         that reg
                             ent presented w
                 on. Th
                             i
         n the nasal cav
         i in the nasal cavity which had breached the
                              i
                         ty wh
                         i
                               ch had breached the
         wall of the orbit and resulted in proptosis.
         wall o f  the orbit and resulted in proptosis.
                                    p
                                     ic Sinonasal
                                  ty
                           p
                            heno
         HPV-related Multi
         HPV-related Multiphenotypic Sinonasal
         Carcinoma Presenting as an Oral Lesion
                               g
         Carcinoma Presenting as an Oral Lesion
         Human Pa  p illoma Virus  ( HPV )  show
         Human Papilloma Virus (HPV) show
         association with many tumours. HPV related
         association with many tumours. HPV related
         multiphenotypic sinonasal carcinoma is a
         multiphenotypic sinonasal carcinoma is a
                                                                 involves the para-testicular region. This patient is a
                                                                 involves the para-testicular region. This patient is a
                                                                 16-year-old male presenting with a right inguino-
                                                                 16-year-old male presenting with a right inguino-
                                                                 scrotal mass for which right high orchidectomy
                                                                 scrotal mass for which right high orchidectomy
                                                                 was done in Barpeta Cancer Centre. The tumour
                                                                 was done in Barpeta Cancer Centre. The tumour
                                                                 cells are spindled and expressed MyoD1.
                                                                 cells are spindled and expressed MyoD1.
                                                                 Vaginal Malignant Melanoma
                                                                 Vaginal Malignant Melanoma
                                                                 Vaginal Malignant Melanoma is a rare entity nant Melanoma is a rare entity
                                                                 Va g inal Mali g
                                                                 constituting 0.3% of all the melanomas. It is an
                                                                 constitutin
                                                                              0.3% of all the melanomas. It is an
                                                                            g
                                                                 aggressive tumour with poor prognosis and affects
                                                                 a gg ressive tumour with poor pro g nosis and affects
                                                                 post-menopausal women. This case is a 58-year-
                                                                 p
                                                                                                                  -
                                                                  ost-menopausal women. This case is a 58-year
                                                                 old female with a lesion in the anterior vaginal wall.
                                                                 old female with a lesion in the anterior va g inal wall.
                                                                 The tumour cells had scant melanin pi
                                                                 The tumour cells had scant melanin pigment in the
                                                                                                       g
                                                                                                                   e
                                                                                                         ment in th
         recently recognised entity in the head and
         recently recognised entity in the head and              cytoplasm and expressed Melan-A.
                                                                 cytoplasm and expressed Melan-A.
         neck region and have a wide morphological
         neck region and have a wide morphological
                                                                                  g
                                                                 Orbital Non-Hod
                                                                 Orbital Non-Hodgkin’s lymphoma (Follicular kin’s lymphoma (Follicular
         spectrum. It closely resembles adenoid cystic
         spectrum. It closely resembles adenoid cystic
                                                                     p
                                                                     p
                                                                   m
                                                                 l lymphoma, low grade)
                                                                  y
                                                                  y
                                                                      homa, low
                                                                                   rade
                                                                                        )
                                                                                 g
                                                                                 g
         carcinoma and needs a thorough evaluation to
         carcinoma and needs a thorough evaluation to
                                                                 Orbital lymphoma / Orbital adnexal lymphomas
                                                                 Orbital lymphoma / Orbital adnexal lymphomas
                                                                 comprise about 10% of malignant orbital tumours.
                                                                 comprise about 10% of malignant orbital tumours.
                                                                 It affects individuals of 5th to 7th decade and
                                                                 It affects individuals of 5th to 7th decade and
         distinguish it from its histological mimics.
         distinguish it from its histological mimics.
         Spindle cell Rhabdomyosarcoma of Para-
         Sp indle cell Rhabdom yo sarcoma of Para-
         testicular Tissue
         testicular Tissue
            ndle cell rhabdom
           i
                                sarcoma
                              yo
                                           s a rare
         Sp
         Spindle cell rhabdomyosarcoma is a rare
                                          i
         variant of embryonal rhabdomyosarcoma
         variant of embryonal rhabdomyosarcoma
         that affects young males and most commonly
         that affects young males and most commonly
          World Cancer Day (2013) theme:(2013) theme:
          World Cancer Da   y
                                                              13
         “Cancer Myths-Get the Facts”
         “Cancer Myths-Get the Facts”
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