Patient-Specific Breast Implant for Breast Reconstruction after Breast-Conserving Mastectomy

20220370183 · 2022-11-24

    Inventors

    Cpc classification

    International classification

    Abstract

    The present invention relates to a patient-specific breast implant. More particularly, the present invention relates to a patient-specific breast implant which, when a breast-conserving surgery (BCS, also called lumpectomy or partial mastectomy) is performed to remove breast cancer while leaving as much normal breast tissue as possible, prevents deformation of breast that may occur due to the depression of breast skin or adhesions of remaining breast tissues after the BCS, shortens surgery time, and facilitates securing breast symmetry, thereby ultimately dramatically increasing the success rate of surgery and maximizing patient satisfaction.

    Claims

    1. A patient-specific breast implant comprising a shell portion constituting an outer wall, the shell portion having a shape complementary to a shape of an inner space secured by a breast tissue expander.

    2. The patient-specific breast implant of claim 1, wherein the shell portion comprises a shape memory polymer.

    3. The patient-specific breast implant of claim 2, wherein the shape memory polymer comprises a polymer material that is changeable in shape according to temperature change.

    4. The patient-specific breast implant of claim 3, wherein the polymer material is any one that is selected from poly-norbornene, polyisoprene, styrene-butadiene copolymer, polyurethane, polyethylene, and polyester-based polymer and which is certified to be harmless when inserted into the human body.

    5. The patient-specific breast implant of claim 4, wherein the polymer material is the polyester-based polymer, and the polyester-based polymer is any one or a combination of two or more that are selected from polyphosphazene, polyanhydride, poly acetal, polyorthoester, polyphosphoester, polyglycolide, poly-ε-caprolactone, polylactide, polycarbonate, and polyamide and which are certified to be harmless when inserted into the human body.

    6. The patient-specific breast implant of claim 2, wherein the shell portion comprises a silicone film made of silicone and a shape memory film made of a shape memory polymer.

    7. The patient-specific breast implant of claim 6, wherein the shape memory film is formed on an outer surface of the silicone film through surface treatment.

    8. The patient-specific breast implant of claim 7, wherein the silicone film is formed through 3D printing.

    9. The patient-specific breast implant of claim 2, wherein the shell portion is made of only the shape memory film and is formed through 3D printing.

    10. The patient-specific breast implant of claim 2, wherein filler and the shell portion are made of only a shape memory polymer.

    11. The patient-specific breast implant of claim 10, wherein filler and the shell portion are made of only a shape memory polymer and are formed through 3D printing.

    12. The patient-specific breast implant of claim 1, further comprising a fixing portion protruding from the surface of the shell portion.

    Description

    DESCRIPTION OF DRAWINGS

    [0056] FIG. 1 is a view illustrating a breast tissue expander according to a conventional art;

    [0057] FIG. 2 is a view illustrating a patient-specific breast implant according to one embodiment of the present invention;

    [0058] FIG. 3 is a view illustrating an original shape, a temporary shape, and a permanent shape of a shape memory polymer;

    [0059] FIG. 4 is a view illustrating a patient-specific breast implant having a shell portion made of only a shape memory film, according to another embodiment of the present invention;

    [0060] FIG. 5 is a view illustrating a patient-specific breast implant made of only a shape memory polymer without using a silicone film or filler, according to a further embodiment of the present invention;

    [0061] FIG. 6 is a view illustrating a patient-specific breast implant according to a further embodiment of the present invention;

    [0062] FIG. 7 is a view illustrating a patient-specific breast implant according to a further embodiment of the present invention;

    [0063] FIG. 8 is a view illustrating a patient-specific breast implant according to a further embodiment of the present invention; and

    [0064] FIG. 9 is a view illustrating a state in which the present invention is used.

    BEST MODE

    [0065] Hereinafter, patient-specific breast implants according to preferred embodiments of the present invention will be described in detail with reference to the accompanying drawings. In describing the present invention, well-known functions or constructions will not be described in detail when it is determined that they may obscure the gist of the present invention. Unless otherwise specified, all terms used in the present specification have the same meaning as the general meaning of the terms understood by a person with ordinary skill in the art to which the present invention belongs, and if the general meaning conflicts with the meaning of a term used in the present specification, the definition used in the present specification is applied.

    [0066] A patient-specific breast implant 1 according to one embodiment of the present invention, when a breast-conserving surgery (BCS, also called lumpectomy or partial mastectomy) is performed to remove breast cancer while leaving as much normal breast tissue as possible, prevents deformation of the breast due to the depression of breast skin or adhesions of remaining breast tissues after the BCS, shortens surgery time, and facilitates securing breast symmetry, thereby ultimately dramatically increasing the success rate of surgery and maximizing patient satisfaction.

    [0067] FIG. 2 is a view illustrating a patient-specific breast implant 1 according to one embodiment of the present invention. Referring to FIG. 2, the patient-specific breast implant 1 includes a shell portion 10.

    [0068] Among components of the patient-specific breast implant 1, the shell portion 10 is a component forming an outer wall. Preferably, the shell portion 10 has a shape complementary to the shape of an inner space S expanded by a breast tissue expander. Therefore, it is possible to shorten the breast reconstruction surgery time, dramatically increase the surgical success rate of the breast reconstruction surgery and avoid sacrificing additional body tissues.

    [0069] The shell portion 10 includes a shape memory polymer. Since the shell portion 10 includes a shape memory polymer, when the patient-specific breast implant 1 having a shape complementary to the shape of a breast tissue removal site after lumpectomy or partial mastectomy is inserted into the body, the shape of the implant 1 can be permanently maintained while the body temperature changes within a body temperature changeable range. This facilitates breast symmetry and enables cosmetically satisfactory breast reconstruction.

    [0070] The shape memory polymer includes a polymer material that is changeable in shape according to temperature change. This polymer material may be any one polymer that is certified to be harmless when inserted into the human body and is selected from among polynorbornene, polyisoprene, styrene-butadiene copolymer, polyurethane, polyethylene, and polyester-based polymers. For this reason, when the patient-specific breast implant 1 is implanted into the body, the shape of the implant 1 can be permanently maintained when the body temperature of the patient is within the normal body temperature range. Therefore, the patient's breast having a similar shape to the original breast can be reconstructed due to the shell portion 10 having a shape complementary to the shape of an area from which the patient's breast is removed.

    [0071] Preferably, the polymer material may be a polyester-based polymer, and the polyester-based polymer may be any one or a combination of two or more that are selected from polyphosphazene, polyanhydride, poly acetal, polyorthoester, polyphosphoester, polyglycolide, poly-ε-caprolactone, polylactide, polycarbonate, and polyamide and which are certified to be harmless when inserted into the human body.

    [0072] Referring to FIG. 2, the shell portion 10 includes a silicone film 11 and a shape memory film 13.

    [0073] The silicone film 11 is a film made of silicone. Preferably, the silicone film 11 may be disposed inside the shape memory film 13 to be described later. A filler F may be disposed inside the silicone film 11. The filler F may be saline. Alternatively, the filler F may be silicone gel or a shape memory polymer certified to be harmless when inserted into the human body. When the filler F is the shape memory polymer, the material disposed outside the shell portion 10 is the same as that of the filler F.

    [0074] The silicone film 11 may be formed by 3D printing. Since the silicone film 11 is formed by 3D printing, a silicone film having a shape complementary to the shape of the breast removed during the breast-conserving surgery (partial mastectomy) can be formed.

    [0075] The shape memory film 13 is a film made of a shape memory polymer. Preferably, the shape memory film 13 may be formed through surface treatment on the outer surface of the silicone film 11. When the entire outer wall of the shell portion 10 is made of a shape memory polymer, the use of a relatively expensive shape memory polymer increases. In this case, the manufacturing cost of the patient-specific breast implant 1 may be dramatically increased. By forming the shape memory film 13 on the outer surface of the silicone film 11 through surface treatment of the silicone film 11, it is possible to reduce the manufacturing cost of the patient-specific breast implant 1. However, the silicone film 11 may not be included and only the shape memory film 13 made of a shape memory polymer may be included to facilitate securing breast symmetry and to enable cosmetically satisfactory breast reconstruction even when a narrow area of depression and skin contracture occur after breast-conserving surgery (i.e., partial mastectomy).

    [0076] In addition, by forming the shape memory film 13 on the outer surface of the silicone film 11 through surface treatment of the silicone film 11, the shape memory film 13 is deformed according to the temperature so that the overall shape of the breast implant is changed to have a shape complementary to the shape of the inner space formed by a breast tissue expander.

    [0077] FIG. 3 is a view illustrating the original shape, a temporary shape, and a permanent shape of the shape memory polymer. Referring to FIG. 3, when it is assumed that the original shape of the shape memory polymer is rectangle as shown in FIG. 3, even though the shape memory polymer is crumpled or rolled to have a temporary shape shown in FIG. 3 due to an external force, the shape memory polymer returns to its original shape at a specific temperature. In the case of a shape memory polymer that returns to the original shape thereof within the body temperature range, the shape memory polymer can maintain the original shape thereof as a permanent shape within the body.

    [0078] FIG. 4 is a view illustrating a patient-specific breast implant 1 having a shell portion made of only a shape memory film, according to another embodiment of the present invention. In this embodiment, the patient-specific breast implant 1 is formed such that the shell portion 10 is made of only a shape memory film 13.

    [0079] That is, the shell portion 10 does not include the silicone film 11 and includes only the shape memory film 13 made of a shape memory polymer, in which the shape memory film 13 constitutes the outer wall of the breast implant 1.

    [0080] In this case, the shell portion 10 may be directly formed through 3D printing using a 3D printing technology. Alternatively, a metal mold having a shape corresponding to a missing portion is first manufactured, and the shape memory film may be formed to have the same shape as the metal mold.

    [0081] Therefore, when the patient-specific breast implant 1 is implanted in a chest region of a patient, the breast implant 1 changes into a shape memorized according to temperature so that the breast implant 1 can be precisely fitted into the inner space secured by a breast tissue expander.

    [0082] FIG. 5 is a view illustrating a patient-specific breast implant composed only of a shape memory polymer without including a silicone film or filler, according to a further embodiment of the present invention. Referring to FIG. 5, the entirety of the patient-specific breast implant 1 is formed of only a shape memory polymer through 3D printing rather than the patient-specific breast implant 1 is formed in a manner that a film is formed first and then the inside of the film is filled with filler. That is, it is possible to construct the patient-specific breast implant 1 in which both the shell portion 10 and the filler F are formed only of a shape memory polymer, and a 3D printing method may be used as a method of manufacturing the same.

    [0083] FIGS. 6 and 7 are views illustrating a patient-specific breast implant according to a further embodiment of the present invention. According to the present embodiment, the patient-specific breast implant 1 includes a fixing portion 30 formed on the shell portion 10. In the case of FIG. 6, the fixing portion 30 is provided on the patient-specific breast implant 1 of FIG. 2. In the case of FIG. 7, the fixing portion 30 is provided on the patient-specific breast implant 1 of FIG. 5. In order to avoid redundant description, only the newly added fixing portion 30 will be described below.

    [0084] The fixing portion 30 protrudes from the surface of the shell portion 10. The fixing portion 30 protruding from the surface of the shell portion 10 serves to fix the breast implant inserted in the inner space secured by a breast tissue expander so that the breast implant may not be rotated or unintentionally moved in the body.

    [0085] Referring to FIGS. 6 and 7, the fixing portion 30 has a hemispherical shape. However, the shape of the fixing portion 30 is not particularly limited. The fixing portion 30 may have any shape if it can have the function described above.

    [0086] In order to improve the fixing effect of the fixing portion 30, preferably, a plurality of fixing portions 30 may be provided on the shell portion 10.

    [0087] FIG. 8 shows a case where the patient-specific breast implant 1 includes neither a silicone film nor filler but is composed of only a shape memory polymer, and the fixing portion 30 is provided on this patient-specific breast implant 1. The patient-specific breast implant 1 may be configured as illustrated in FIG. 8. Alternatively, the fixing portion 30 as well as the patient-specific breast implant 1 may be made of a shape memory polymer. In this case, the patient-specific breast implant 1 and the fixing portion 30 are both formed through 3D printing.

    [0088] FIG. 9 is a view illustrating a state in which the present invention is used. Referring to FIG. 9, when a breast-conserving surgery (i.e., partial mastectomy) that minimizes the removal of the surrounding healthy tissue is performed, a small breast tissue expander is inserted into the area where the breast has been removed, and the inner space S is enlarged by expanding only the tissue in the desired area.

    [0089] Thereafter, the patient-specific breast implant 1 having a shape complementary to the shape of the inner space S created by the small breast tissue expander is inserted into the inner space S. The breast implant 1 may completely fill the inner space S. As a result, the contour of the entire breast is not distorted, and a breast with a shape similar to the original breast shape can be reconstructed cosmetically.

    [0090] The above detailed description is illustrative of the present invention. In addition, the above description shows and describes preferred embodiments of the present invention, and the present invention may be used in various environments such that various embodiments are diversely combined or modified. That is, various changes or modifications to the embodiments are possible without departing from the scope of the concept of the invention disclosed herein, the scope equivalent to the written disclosure, and/or the scope of skill or knowledge in the relevant art. The embodiments are provided to describe the best state for implementing the technical idea of the present invention, and various changes required in the specific applications and uses of the present invention are possible. Therefore, the detailed description of the present disclosure is not intended to limit the present invention to the disclosed embodiments. The appended claims should be construed as including other embodiments.