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m355

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      m355
      Participant

        sorry to hear the news.  I know it can be discouraging but hopefully there is something else out there that you respond better to.  Praying for you!

        m355
        Participant

          sorry to hear the news.  I know it can be discouraging but hopefully there is something else out there that you respond better to.  Praying for you!

          m355
          Participant

            sorry to hear the news.  I know it can be discouraging but hopefully there is something else out there that you respond better to.  Praying for you!

            m355
            Participant

              would you consider have the pathology slides sent to another dermapathologist for a consult? I do it all the time!

              m355
              Participant

                would you consider have the pathology slides sent to another dermapathologist for a consult? I do it all the time!

                m355
                Participant

                  would you consider have the pathology slides sent to another dermapathologist for a consult? I do it all the time!

                  m355
                  Participant

                    this is my 3rd melanoma. given it is my 3rd, the derm, pathologist and oncologist said it is something to consider.  and here is the most recent report:

                    Here is lab report:

                    A) Skin, right upper back, punch biopsy: Severely
                    atypical compound melanocytic proliferation, see
                    Comment.

                    COMMENT:
                    This is a worrisome lesion, with epidermal atypia
                    (pagetoid extension, confluent growth) consistent with
                    melanoma in situ and a dermal component that also
                    demonstrates atypia with areas of morphologically
                    similar cells to the epidermal component, but also some
                     reassuring features (dispersion with increasing dermal
                     depth, absence of mitoses). These findings engender a
                    differential diagnosis that could reasonably include
                    melanoma in situ evolving within a dysplastic nevus or
                    a superfically invasive melanoma. Given this
                    differential, it would be reasonable to treat this
                    lesion as if it represents a malignant melanoma with
                    the following prognostic factors: Breslow depth 0.32mm,
                     Clark's level II, 0 mitoses/mm2, no ulceration.
                     

                    MICROSCOPIC DESCRIPTION:
                    A) Sections show a punch biopsy with a compound
                    melanocytic proliferation. The junctional component
                    shows crowding, with fusion between adjacent rete and
                    horizontal nests. Areas of upward extension of single
                    melanocytes and nests are seen, and highlighted by
                    Melan-A. Intraepidermal melanocytes show cytologic
                    atypia, with nuclear enlargement and abundant
                    cytoplasm. A patchy lymphohistiocytic inflammatory
                    infiltrate is present. The lesion is free of the punch
                    biopsy margin. Additional step sections are examined.

                     

                    m355
                    Participant

                      this is my 3rd melanoma. given it is my 3rd, the derm, pathologist and oncologist said it is something to consider.  and here is the most recent report:

                      Here is lab report:

                      A) Skin, right upper back, punch biopsy: Severely
                      atypical compound melanocytic proliferation, see
                      Comment.

                      COMMENT:
                      This is a worrisome lesion, with epidermal atypia
                      (pagetoid extension, confluent growth) consistent with
                      melanoma in situ and a dermal component that also
                      demonstrates atypia with areas of morphologically
                      similar cells to the epidermal component, but also some
                       reassuring features (dispersion with increasing dermal
                       depth, absence of mitoses). These findings engender a
                      differential diagnosis that could reasonably include
                      melanoma in situ evolving within a dysplastic nevus or
                      a superfically invasive melanoma. Given this
                      differential, it would be reasonable to treat this
                      lesion as if it represents a malignant melanoma with
                      the following prognostic factors: Breslow depth 0.32mm,
                       Clark's level II, 0 mitoses/mm2, no ulceration.
                       

                      MICROSCOPIC DESCRIPTION:
                      A) Sections show a punch biopsy with a compound
                      melanocytic proliferation. The junctional component
                      shows crowding, with fusion between adjacent rete and
                      horizontal nests. Areas of upward extension of single
                      melanocytes and nests are seen, and highlighted by
                      Melan-A. Intraepidermal melanocytes show cytologic
                      atypia, with nuclear enlargement and abundant
                      cytoplasm. A patchy lymphohistiocytic inflammatory
                      infiltrate is present. The lesion is free of the punch
                      biopsy margin. Additional step sections are examined.

                       

                      m355
                      Participant

                        this is my 3rd melanoma. given it is my 3rd, the derm, pathologist and oncologist said it is something to consider.  and here is the most recent report:

                        Here is lab report:

                        A) Skin, right upper back, punch biopsy: Severely
                        atypical compound melanocytic proliferation, see
                        Comment.

                        COMMENT:
                        This is a worrisome lesion, with epidermal atypia
                        (pagetoid extension, confluent growth) consistent with
                        melanoma in situ and a dermal component that also
                        demonstrates atypia with areas of morphologically
                        similar cells to the epidermal component, but also some
                         reassuring features (dispersion with increasing dermal
                         depth, absence of mitoses). These findings engender a
                        differential diagnosis that could reasonably include
                        melanoma in situ evolving within a dysplastic nevus or
                        a superfically invasive melanoma. Given this
                        differential, it would be reasonable to treat this
                        lesion as if it represents a malignant melanoma with
                        the following prognostic factors: Breslow depth 0.32mm,
                         Clark's level II, 0 mitoses/mm2, no ulceration.
                         

                        MICROSCOPIC DESCRIPTION:
                        A) Sections show a punch biopsy with a compound
                        melanocytic proliferation. The junctional component
                        shows crowding, with fusion between adjacent rete and
                        horizontal nests. Areas of upward extension of single
                        melanocytes and nests are seen, and highlighted by
                        Melan-A. Intraepidermal melanocytes show cytologic
                        atypia, with nuclear enlargement and abundant
                        cytoplasm. A patchy lymphohistiocytic inflammatory
                        infiltrate is present. The lesion is free of the punch
                        biopsy margin. Additional step sections are examined.

                         

                        m355
                        Participant

                          I do make alot of atypical moles that is for sure.  But nothing crazy, crazy are the normal ones that go rogue. My thoughts exactly if there was to ever be a treatment advantage.

                          m355
                          Participant

                            I do make alot of atypical moles that is for sure.  But nothing crazy, crazy are the normal ones that go rogue. My thoughts exactly if there was to ever be a treatment advantage.

                            m355
                            Participant

                              I do make alot of atypical moles that is for sure.  But nothing crazy, crazy are the normal ones that go rogue. My thoughts exactly if there was to ever be a treatment advantage.

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