A 32 year old female presented with a rigid left middle finger with no visible skin crease over the DIP joint. Discuss the relevant investigations, the possible diagnosis and the management of the case.
Patient was referred by her GP for a consultation regarding a rigid left middle finger, which she'd had since birth. On examination it was noted that the left middle finger was of normal length but there was no skin crease over the DIP joint, and clinically no movement was possible at the joint. An X-ray revealed fusion of the DIP joint.
Symphalangism is a rare congenital disorder in which there is fusion of the interphalangeal joints.Involvement of the DIP joint is sporadic but PIP joint involvement has been described with a number of congenital anomalies and the mode of inheritance is autosomal dominant. The associated anomalies include spinal, carpal and tarsal fusion as well as conduction deafness. The patient usually presents with a stiff finger. Examination will reveal absence of skin creases over the affected joint (Fig 1). Radiologically, the findings are bony ankylosis(Fig 2), minimal joint space and sometimes the digit is shorter than normal. In a patient with distal symphalangism,no treatment is recommended to restore motion to the DIP joint, as the dysfunction is not significant.
Symphalangia of the Distal interphalangeal joint
Based on the provided hand X-ray examinations, the following features are observed:
Taking into account the patient's history (present since childhood or congenital, with no obvious history of trauma) and current radiological findings, the following diagnoses or differential diagnoses may be considered:
Considering the patient's age, clinical manifestations (finger stiffness, absence of skin creases over the joint), and the X-ray findings of bony fusion in the distal interphalangeal joint, the most likely diagnosis is:
Congenital symphalangism of the distal interphalangeal joint (congenital interphalangeal ankylosis).
If further confirmation is needed, a family history investigation or genetic testing can be performed to determine any congenital or hereditary factors. However, in most cases, clinical imaging and history are sufficient for diagnosis.
Because movement of the distal interphalangeal joint has a relatively minor impact on overall hand function, the primary goal of rehabilitation is to maintain the flexibility of other joints and overall hand function. The following progressive plan may be considered:
Throughout the rehabilitation process, training frequency, intensity, and methods should be adjusted individually, and each session should be gradually extended to suit the patient's specific condition. If persistent pain or significant functional decline occurs, seek medical review in a timely manner.
Disclaimer: This report is for reference based on the provided information and does not replace a clinical diagnosis or in-person guidance from a medical professional. If the patient has any questions or experiences worsening symptoms, they should promptly consult a specialist and undergo an in-person examination.
Symphalangia of the Distal interphalangeal joint