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Página Diaphyseal Aclasise                                                                    1 de 3




        Diaphyseal Aclasis

   Definition
   Hereditary multiple exostoses,
   Also known as..
   Diaphyseal Aclasis
   External Chondromatosis Syndrome
   Multiple Cartilaginous Exostoses
   Multiple Exostoses
   Multiple Exostoses Syndrome
   Multiple Osteochondromatosis

   Radiographic Appearance
   Due to the widespread nature of the disease a limited skeletal survey may need to be
   performed with additional modalities eg CT of areas with severe symptoms.

   Pathology
   Hereditary Multiple Exostoses (HME) is a rare skeletal disorder that is inherited in an
   autosomal dominant fashion. As the name suggests, this disorder is characterized by multiple
   bony growths or tumors (exostoses), often on the growing end (epiphysis) of the long bones
   of the legs, arms, and digits. These bony growths are covered by cartilage and usually
   continue to grow until shortly after puberty. They may cause deformities, especially of the
   ankle, knee, and wrist
   Although any bone can be affected, the long bones (legs, arms, fingers, toes), pelvis and
   shoulder blades are the most common, while the face and skull are generally unaffected.
   Boys and girls can both be affected. Older literature claimed that boys were more severely
   troubled by MHE, but bigger series of patients studied recently do not support this theory

   MHE can be troublesome. Because the exostoses grow near the growth centers of the bone,
   they can make the growth center grow poorly, or only part of it grow poorly. This makes a lot
   of people with MHE somewhat shorter than average or have bowed arms or legs. Often, the
   forearm will bow out toward the lime finger, or the legs can become knock kneed. This is
   frequently concerning, but function is often normal though cosmetically, the bowing can be
   very troubling. Sometimes folks with MHE get stiff, especially in the elbows and hips,
   usually because their exostoses block some of their motion. While children are growing,
   exostoses can be painful. They seem to be very sensitive to getting bumped. Kids often
   develop exostoses on the inside of their knees and these can hit together when they run,
   which hurts!

   Sometimes exostoses grow near nerves or tendons and press on them. In these cases, they
   often need to be removed so they won't damage the structure laying over them.

   The most frightening complication of MHE is also one of the most uncommon. Rarely (less
   than 1% of the time), the benign exostoses of MHE can become a malignant tumor called
   chondrosarcoma. This happens almost always after adulthood when skeletal growth has
   ceased. Usually, patients who develop chondrosarcoma are in their 20's to 50's. If a person
   with MHE notices that an exostoses is getting bigger or painful after they have stopped
   growing they should get to their doctor! Growth and pain are two important warning signs
   that a benign tumor has become malignant. Chondrosarcoma is very rare, but it is something
   MHE families must know about


   Treatment:
   Some people with MHE never require any treatment. They learn to compensate for deformity



http://www.e-radiography.net/radpath/d/diaphyseal_aclasis.htm                             28-02-2012
Página Diaphyseal Aclasise                                                                            2 de 3




   or decreased range of motion so they function normally. When deformity does occur, it often
   happens so slowly that the patient can compensate for it well, while others may require
   surgery to help them.

   If an exostoses is painful, pressing on an important structure, cosmetically unattractive or if
   easily bumped, it can be surgically removed. Once removed, exostoses can reoccur (about 20
   - 50% of the time), but may not regrow to a size large enough to be symptomatic. Removal
   itself is usually a fairly small procedure; some are removed without ever staying overnight in
   the hospital.

   If an exostoses causes a growth abnormality, like bowing, sometimes just removing the
   exostoses early enough will allow the bone to straighten itself out and remodel as the child
   grows. Some bowing is so severe that not only must the exostoses be removed, but also the
   bone must be straightened. This can be done by either cutting the bone, straightening it and
   then holding it in place while it heals or if the child is still growing by changing the rate of
   growth on one side of the growth plate. Currently there are several options and your doctor
   should be able to explain them to you.

   If an exostoses does become malignant and turn into a chondrosarcoma then it must be
   removed. A specialist in orthopedics and bone tumors would be required to help with this.

   Images




   http://www.rad.washington.edu




   Useful Link: http://members.tripod.com/MOONROSE_22/



http://www.e-radiography.net/radpath/d/diaphyseal_aclasis.htm                                28-02-2012
Página Diaphyseal Aclasise                                          3 de 3




http://www.e-radiography.net/radpath/d/diaphyseal_aclasis.htm   28-02-2012

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Diaphyseal aclasis

  • 1. Página Diaphyseal Aclasise 1 de 3 Diaphyseal Aclasis Definition Hereditary multiple exostoses, Also known as.. Diaphyseal Aclasis External Chondromatosis Syndrome Multiple Cartilaginous Exostoses Multiple Exostoses Multiple Exostoses Syndrome Multiple Osteochondromatosis Radiographic Appearance Due to the widespread nature of the disease a limited skeletal survey may need to be performed with additional modalities eg CT of areas with severe symptoms. Pathology Hereditary Multiple Exostoses (HME) is a rare skeletal disorder that is inherited in an autosomal dominant fashion. As the name suggests, this disorder is characterized by multiple bony growths or tumors (exostoses), often on the growing end (epiphysis) of the long bones of the legs, arms, and digits. These bony growths are covered by cartilage and usually continue to grow until shortly after puberty. They may cause deformities, especially of the ankle, knee, and wrist Although any bone can be affected, the long bones (legs, arms, fingers, toes), pelvis and shoulder blades are the most common, while the face and skull are generally unaffected. Boys and girls can both be affected. Older literature claimed that boys were more severely troubled by MHE, but bigger series of patients studied recently do not support this theory MHE can be troublesome. Because the exostoses grow near the growth centers of the bone, they can make the growth center grow poorly, or only part of it grow poorly. This makes a lot of people with MHE somewhat shorter than average or have bowed arms or legs. Often, the forearm will bow out toward the lime finger, or the legs can become knock kneed. This is frequently concerning, but function is often normal though cosmetically, the bowing can be very troubling. Sometimes folks with MHE get stiff, especially in the elbows and hips, usually because their exostoses block some of their motion. While children are growing, exostoses can be painful. They seem to be very sensitive to getting bumped. Kids often develop exostoses on the inside of their knees and these can hit together when they run, which hurts! Sometimes exostoses grow near nerves or tendons and press on them. In these cases, they often need to be removed so they won't damage the structure laying over them. The most frightening complication of MHE is also one of the most uncommon. Rarely (less than 1% of the time), the benign exostoses of MHE can become a malignant tumor called chondrosarcoma. This happens almost always after adulthood when skeletal growth has ceased. Usually, patients who develop chondrosarcoma are in their 20's to 50's. If a person with MHE notices that an exostoses is getting bigger or painful after they have stopped growing they should get to their doctor! Growth and pain are two important warning signs that a benign tumor has become malignant. Chondrosarcoma is very rare, but it is something MHE families must know about Treatment: Some people with MHE never require any treatment. They learn to compensate for deformity http://www.e-radiography.net/radpath/d/diaphyseal_aclasis.htm 28-02-2012
  • 2. Página Diaphyseal Aclasise 2 de 3 or decreased range of motion so they function normally. When deformity does occur, it often happens so slowly that the patient can compensate for it well, while others may require surgery to help them. If an exostoses is painful, pressing on an important structure, cosmetically unattractive or if easily bumped, it can be surgically removed. Once removed, exostoses can reoccur (about 20 - 50% of the time), but may not regrow to a size large enough to be symptomatic. Removal itself is usually a fairly small procedure; some are removed without ever staying overnight in the hospital. If an exostoses causes a growth abnormality, like bowing, sometimes just removing the exostoses early enough will allow the bone to straighten itself out and remodel as the child grows. Some bowing is so severe that not only must the exostoses be removed, but also the bone must be straightened. This can be done by either cutting the bone, straightening it and then holding it in place while it heals or if the child is still growing by changing the rate of growth on one side of the growth plate. Currently there are several options and your doctor should be able to explain them to you. If an exostoses does become malignant and turn into a chondrosarcoma then it must be removed. A specialist in orthopedics and bone tumors would be required to help with this. Images http://www.rad.washington.edu Useful Link: http://members.tripod.com/MOONROSE_22/ http://www.e-radiography.net/radpath/d/diaphyseal_aclasis.htm 28-02-2012
  • 3. Página Diaphyseal Aclasise 3 de 3 http://www.e-radiography.net/radpath/d/diaphyseal_aclasis.htm 28-02-2012